+1 858-523-8231
Login | Register
menu
AA Blocks, Building Blocks, Catalysts, Inhibitors
Login | Register
18328-11-5,MFCD00800383
Catalog No.:AA0027E6

18328-11-5 | 4-Phenylbutyraldehyde

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
97%
in stock  
$170.00   $119.00
- +
5g
97%
in stock  
$502.00   $352.00
- +
10g
97%
in stock  
$809.00   $567.00
- +
25g
97%
in stock  
$1,607.00 $1,125.00
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0027E6
Chemical Name:
4-Phenylbutyraldehyde
CAS Number:
18328-11-5
Molecular Formula:
C10H12O
Molecular Weight:
148.2017
MDL Number:
MFCD00800383
SMILES:
O=CCCCc1ccccc1
Properties
Computed Properties
 
Complexity:
103  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
1  
Rotatable Bond Count:
4  
XLogP3:
2  

Downstream Synthesis Route

[1]ChemischeBerichte,1912,vol.45,p.396

[1]TetrahedronLetters,2011,vol.52,p.422-425

[2]Patent:WO2013/102242,2013,A1.Locationinpatent:Page/Pagecolumn119;120

[3]Bioorganicandmedicinalchemistry,1999,vol.7,p.3003-3009

[4]JournaloftheChemicalSociety.PerkinTransactions2(2001),1997,p.1585-1596

[5]Patent:US2003/225059,2003,A1.Locationinpatent:Page23

[6]Synlett,2017,vol.28,p.1554-1557

[7]ChemicalandPharmaceuticalBulletin,2011,vol.59,p.1570-1573

[8]Patent:EP2085373,2009,A1.Locationinpatent:Page/Pagecolumn11;14-15

[9]Patent:EP2594550,2013,A1.Locationinpatent:Paragraph0059;0060

[10]JournalofMedicinalChemistry,1982,vol.25,p.1189-1192

[11]JournalofChemicalResearch-PartS,2002,p.270-271

[12]JournaloftheAmericanChemicalSociety,2009,vol.131,p.251-262

[13]SyntheticCommunications,2014,vol.44,p.589-599

[14]Patent:WO2008/46071,2008,A2.Locationinpatent:Page/Pagecolumn51

[15]Patent:WO2008/31032,2008,A2.Locationinpatent:Page/Pagecolumn50-51

[16]AngewandteChemie-InternationalEdition,2013,vol.52,p.12624-12627    Angew.Chem.,2013,vol.125,p.12856-12859,4

[17]Chemistry-AEuropeanJournal,2020,vol.26,p.1249-1253

[18]JournalofOrganicChemistry,2012,vol.77,p.3005-3009

[19]Chemistry-AEuropeanJournal,2004,vol.10,p.4206-4213

[20]AngewandteChemie-InternationalEdition,2015,vol.54,p.4208-4211    Angew.Chem.,2015,vol.127,p.4282-4285,4

[21]JournaloftheAmericanChemicalSociety,1996,vol.118,p.502-508

[22]Synlett,2006,p.2055-2058

[23]OrganicLetters,2013,vol.15,p.992-995

[24]AngewandteChemie-InternationalEdition,2019,vol.58,p.6385-6390    Angew.Chem.,2019,vol.131,p.6451-6456,6

[25]JournalofOrganicChemistry,2014,vol.79,p.10256-10268

[26]AustralianJournalofChemistry,2008,vol.61,p.930-940

[27]JournaloftheAmericanChemicalSociety,2011,vol.133,p.6497-6500

[28]SyntheticCommunications,2012,vol.42,p.1731-1745

[29]OrganicProcessResearchandDevelopment,2019,vol.23,p.571-577

[30]JournalofOrganicChemistry,2004,vol.69,p.8676-8680

[31]Patent:US2006/79562,2006,A1.Locationinpatent:Page/Pagecolumn19

[32]JournaloftheChemicalSociety.PerkintransactionsII,1984,p.1833-1842

[33]Patent:WO2009/152082,2009,A1.Locationinpatent:Page/Pagecolumn184

[34]JournalofOrganicChemistry,1990,vol.55,p.2045-2055

[35]JournalofOrganicChemistry,1992,vol.57,p.5785-5787

[36]SyntheticCommunications,2016,vol.46,p.885-892

[37]Patent:EP1502916,2005,A1.Locationinpatent:Page424

[38]OrganicandBiomolecularChemistry,2017,vol.15,p.2609-2628

[39]HeteroatomChemistry,2019,vol.2019

[40]Patent:WO2008/643,2008,A1.Locationinpatent:Page/Pagecolumn69

[41]JournalofOrganicChemistry,1996,vol.61,p.1578-1598

[42]EuropeanJournalofMedicinalChemistry,1996,vol.31,p.683-692

[43]TetrahedronAsymmetry,1999,vol.10,p.3939-3949

[44]Bioorganicandmedicinalchemistryletters,2003,vol.13,p.293-295

[45]OrganicLetters,2004,vol.6,p.1883-1886

[46]Synlett,2004,p.2010-2012

[47]AngewandteChemie-InternationalEdition,2006,vol.45,p.4776-4779

[48]JournalofOrganicChemistry,2002,vol.67,p.8758-8763

[49]AngewandteChemie-InternationalEdition,2007,vol.46,p.7210-7213

[50]JournaloftheAmericanChemicalSociety,2009,vol.131,p.16017-16020

[51]OrganicLetters,2010,vol.12,p.532-535

[52]Patent:WO2012/69605,2012,A1.Locationinpatent:Page/Pagecolumn58

[53]AngewandteChemie-InternationalEdition,2012,vol.51,p.6187-6190

[54]Chemistry-AEuropeanJournal,2012,vol.18,p.13520-13530

[55]JournalofMedicinalChemistry,2014,vol.57,p.1790-1801

[56]OrganicLetters,2014,vol.16,p.2026-2029

[57]SyntheticCommunications,2014,vol.44,p.2818-2825

[58]RSCAdvances,2014,vol.4,p.44039-44042

[59]JournalofOrganicChemistry,2016,vol.81,p.2189-2193

[60]RSCAdvances,2016,vol.6,p.35008-35013

[61]JournalofOrganicChemistry,2015,vol.80,p.401-413

[62]ChemSusChem,2014,vol.7,p.2684-2689

[63]Chemistry-AEuropeanJournal,2017,vol.23,p.10276-10279

[64]Patent:CN106800492,2017,A.Locationinpatent:Paragraph0037;0038;0039

[65]MedicinalChemistry,2017,vol.13,p.65-76

[66]AngewandteChemie-InternationalEdition,2017,vol.56,p.15599-15602    Angew.Chem.,2017,vol.129,p.15805-15808,4

[67]JournalofMaterialsChemistryA,2018,vol.6,p.9860-9865

[68]AngewandteChemie-InternationalEdition,2018,vol.57,p.12921-12924    Angew.Chem.,2018,vol.130,p.13103-13106,4

[69]Patent:WO2005/25498,2005,A2.Locationinpatent:Page/Pagecolumn36

[70]Patent:WO2018/201192,2018,A1.Locationinpatent:Page/Pagecolumn52-53

[71]EuropeanJournalofOrganicChemistry,2019,vol.2019,p.3190-3194

[72]AngewandteChemie-InternationalEdition,2020,vol.59,p.2360-2364    Angew.Chem.,2020,vol.132,p.2380-2384,5

[73]AngewandteChemie-InternationalEdition,2020,vol.59,p.11010-11019    Angew.Chem.,2020,vol.132,p.11103-11112,10

[1]Fujihara,Tetsuaki;Cong,Cong;Terao,Jun;Tsuji,Yasushi[AdvancedSynthesisandCatalysis,2013,vol.355,#17,p.3420-3424]

[2]Aggarwal,VarinderK.;Noble,Adam;Tyler,JasperL.[AngewandteChemie-InternationalEdition,2022,vol.61,#3][Angew.Chem.,2022,vol.134,#3]

[3]Angle,StevenR.;Arnaiz,DamianO.;Boyce,JamesP.;Frutos,RogelioP.;Louie,MichaelS.;etal.[JournalofOrganicChemistry,1994,vol.59,#21,p.6322-6337]

[4]Salvino,JosephM.;Mervic,Miljenko;Mason,HelenJ.;Kiesow,Terence;Teager,David;Airey,John;Labaudiniere,Richard[JournalofOrganicChemistry,1999,vol.64,#6,p.1823-1830]

[5]Roda,Gabriella;Riva,Sergio;Danieli,Bruno[TetrahedronAsymmetry,1999,vol.10,#20,p.3939-3949]

[6]Kawakami;Kitani;Yuasa;Abe;Moriwaki;Kagoshima;Terasawa;Tahara[EuropeanJournalofMedicinalChemistry,1996,vol.31,#9,p.683-692]

[7]Penn,JohnH.;Liu,Fang[JournalofOrganicChemistry,1994,vol.59,#9,p.2608-2612]

[8]Ellis-Davies,GrahamC.R.;Gilbert,Andrew;Heath,Peter;Lane,JonC.;Warrington,JohnV.;Westover,DavidL.[JournaloftheChemicalSociety.PerkintransactionsII,1984,p.1833-1842]

[9]Fujihara,Tetsuaki;Cong,Cong;Iwai,Tomohiro;Terao,Jun;Tsuji,Yasushi[Synlett,2012,vol.23,#16,p.2389-2392]

[10]Duan,Yitao;Yao,Peiyuan;Chen,Xi;Liu,Xiangtao;Zhang,Rui;Feng,Jinhui;Wu,Qiaqing;Zhu,Dunming[JournalofMolecularCatalysisB:Enzymatic,2015,vol.115,p.1-7]

[11]Shimogaki,Mio;Fujita,Morifumi;Sugimura,Takashi[AngewandteChemie-InternationalEdition,2016,vol.55,#51,p.15797-15801][Angew.Chem.,2016,vol.128,p.16029-16033,5]

[12]Shiely,AmyE.;Slattery,CatherineN.;Ford,Alan;Eccles,KevinS.;Lawrence,SimonE.;Maguire,AnitaR.[OrganicandBiomolecularChemistry,2017,vol.15,#12,p.2609-2628]

[13]Nouaille,Augustin;Pannecoucke,Xavier;Poisson,Thomas;Couve-Bonnaire,Samuel[AdvancedSynthesisandCatalysis,2021,vol.363,#8,p.2140-2147]

[1]Kawakami;Kitani;Yuasa;Abe;Moriwaki;Kagoshima;Terasawa;Tahara[EuropeanJournalofMedicinalChemistry,1996,vol.31,#9,p.683-692]

[1]Patent:US2006/79562,2006,A1.Locationinpatent:Page/Pagecolumn19

[2]ActaChemicaScandinavica,1999,vol.53,p.792-799

Literature

Title: Inversion of stereoselectivity by applying mutants of the hydroxynitrile lyase from Manihot esculenta.

Journal: Chembiochem : a European journal of chemical biology 20050401

Title: Conformationally rigid N-acyl-5-alkyl-L-prolyl-pyrrolidines as prolyl oligopeptidase inhibitors.

Journal: Bioorganic & medicinal chemistry 20030815

Title: Non-thiol farnesyltransferase inhibitors: structure-activity relationships of aralkylsubstituted benzophenones.

Journal: Archiv der Pharmazie 20010201

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
Submit
SDS
Related Products of 18328-11-5
1007-32-5

1007-32-5

 1009-14-9

1009-14-9

 1199-98-0

1199-98-0

 1466-74-6

1466-74-6

 1469-83-6

1469-83-6

 14721-44-9

14721-44-9
Building Blocks
More >
Tags:18328-11-5 Molecular Formula|18328-11-5 MDL|18328-11-5 SMILES|18328-11-5 4-Phenylbutyraldehyde
Catalog No.: AA0027E6
18328-11-5,MFCD00800383
18328-11-5 | 4-Phenylbutyraldehyde
Pack Size： 1g
Purity： 97%
in stock
$170.00 $119.00
Pack Size： 5g
Purity： 97%
in stock
$502.00 $352.00
Pack Size： 10g
Purity： 97%
in stock
$809.00 $567.00
Pack Size： 25g
Purity： 97%
in stock
$1,607.00 $1,125.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA0027E6
Chemical Name: 4-Phenylbutyraldehyde
CAS Number: 18328-11-5
Molecular Formula: C10H12O
Molecular Weight: 148.2017
MDL Number: MFCD00800383
SMILES: O=CCCCc1ccccc1
Properties
Complexity: 103  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 1  
Rotatable Bond Count: 4  
XLogP3: 2  
Downstream Synthesis Route
34993-02-7    18328-11-5 

[1]ChemischeBerichte,1912,vol.45,p.396

3360-41-6    18328-11-5 

[1]TetrahedronLetters,2011,vol.52,p.422-425

[2]Patent:WO2013/102242,2013,A1.Locationinpatent:Page/Pagecolumn119;120

[3]Bioorganicandmedicinalchemistry,1999,vol.7,p.3003-3009

[4]JournaloftheChemicalSociety.PerkinTransactions2(2001),1997,p.1585-1596

[5]Patent:US2003/225059,2003,A1.Locationinpatent:Page23

[6]Synlett,2017,vol.28,p.1554-1557

[7]ChemicalandPharmaceuticalBulletin,2011,vol.59,p.1570-1573

[8]Patent:EP2085373,2009,A1.Locationinpatent:Page/Pagecolumn11;14-15

[9]Patent:EP2594550,2013,A1.Locationinpatent:Paragraph0059;0060

[10]JournalofMedicinalChemistry,1982,vol.25,p.1189-1192

[11]JournalofChemicalResearch-PartS,2002,p.270-271

[12]JournaloftheAmericanChemicalSociety,2009,vol.131,p.251-262

[13]SyntheticCommunications,2014,vol.44,p.589-599

[14]Patent:WO2008/46071,2008,A2.Locationinpatent:Page/Pagecolumn51

[15]Patent:WO2008/31032,2008,A2.Locationinpatent:Page/Pagecolumn50-51

[16]AngewandteChemie-InternationalEdition,2013,vol.52,p.12624-12627    Angew.Chem.,2013,vol.125,p.12856-12859,4

[17]Chemistry-AEuropeanJournal,2020,vol.26,p.1249-1253

[18]JournalofOrganicChemistry,2012,vol.77,p.3005-3009

[19]Chemistry-AEuropeanJournal,2004,vol.10,p.4206-4213

[20]AngewandteChemie-InternationalEdition,2015,vol.54,p.4208-4211    Angew.Chem.,2015,vol.127,p.4282-4285,4

[21]JournaloftheAmericanChemicalSociety,1996,vol.118,p.502-508

[22]Synlett,2006,p.2055-2058

[23]OrganicLetters,2013,vol.15,p.992-995

[24]AngewandteChemie-InternationalEdition,2019,vol.58,p.6385-6390    Angew.Chem.,2019,vol.131,p.6451-6456,6

[25]JournalofOrganicChemistry,2014,vol.79,p.10256-10268

[26]AustralianJournalofChemistry,2008,vol.61,p.930-940

[27]JournaloftheAmericanChemicalSociety,2011,vol.133,p.6497-6500

[28]SyntheticCommunications,2012,vol.42,p.1731-1745

[29]OrganicProcessResearchandDevelopment,2019,vol.23,p.571-577

[30]JournalofOrganicChemistry,2004,vol.69,p.8676-8680

[31]Patent:US2006/79562,2006,A1.Locationinpatent:Page/Pagecolumn19

[32]JournaloftheChemicalSociety.PerkintransactionsII,1984,p.1833-1842

[33]Patent:WO2009/152082,2009,A1.Locationinpatent:Page/Pagecolumn184

[34]JournalofOrganicChemistry,1990,vol.55,p.2045-2055

[35]JournalofOrganicChemistry,1992,vol.57,p.5785-5787

[36]SyntheticCommunications,2016,vol.46,p.885-892

[37]Patent:EP1502916,2005,A1.Locationinpatent:Page424

[38]OrganicandBiomolecularChemistry,2017,vol.15,p.2609-2628

[39]HeteroatomChemistry,2019,vol.2019

[40]Patent:WO2008/643,2008,A1.Locationinpatent:Page/Pagecolumn69

[41]JournalofOrganicChemistry,1996,vol.61,p.1578-1598

[42]EuropeanJournalofMedicinalChemistry,1996,vol.31,p.683-692

[43]TetrahedronAsymmetry,1999,vol.10,p.3939-3949

[44]Bioorganicandmedicinalchemistryletters,2003,vol.13,p.293-295

[45]OrganicLetters,2004,vol.6,p.1883-1886

[46]Synlett,2004,p.2010-2012

[47]AngewandteChemie-InternationalEdition,2006,vol.45,p.4776-4779

[48]JournalofOrganicChemistry,2002,vol.67,p.8758-8763

[49]AngewandteChemie-InternationalEdition,2007,vol.46,p.7210-7213

[50]JournaloftheAmericanChemicalSociety,2009,vol.131,p.16017-16020

[51]OrganicLetters,2010,vol.12,p.532-535

[52]Patent:WO2012/69605,2012,A1.Locationinpatent:Page/Pagecolumn58

[53]AngewandteChemie-InternationalEdition,2012,vol.51,p.6187-6190

[54]Chemistry-AEuropeanJournal,2012,vol.18,p.13520-13530

[55]JournalofMedicinalChemistry,2014,vol.57,p.1790-1801

[56]OrganicLetters,2014,vol.16,p.2026-2029

[57]SyntheticCommunications,2014,vol.44,p.2818-2825

[58]RSCAdvances,2014,vol.4,p.44039-44042

[59]JournalofOrganicChemistry,2016,vol.81,p.2189-2193

[60]RSCAdvances,2016,vol.6,p.35008-35013

[61]JournalofOrganicChemistry,2015,vol.80,p.401-413

[62]ChemSusChem,2014,vol.7,p.2684-2689

[63]Chemistry-AEuropeanJournal,2017,vol.23,p.10276-10279

[64]Patent:CN106800492,2017,A.Locationinpatent:Paragraph0037;0038;0039

[65]MedicinalChemistry,2017,vol.13,p.65-76

[66]AngewandteChemie-InternationalEdition,2017,vol.56,p.15599-15602    Angew.Chem.,2017,vol.129,p.15805-15808,4

[67]JournalofMaterialsChemistryA,2018,vol.6,p.9860-9865

[68]AngewandteChemie-InternationalEdition,2018,vol.57,p.12921-12924    Angew.Chem.,2018,vol.130,p.13103-13106,4

[69]Patent:WO2005/25498,2005,A2.Locationinpatent:Page/Pagecolumn36

[70]Patent:WO2018/201192,2018,A1.Locationinpatent:Page/Pagecolumn52-53

[71]EuropeanJournalofOrganicChemistry,2019,vol.2019,p.3190-3194

[72]AngewandteChemie-InternationalEdition,2020,vol.59,p.2360-2364    Angew.Chem.,2020,vol.132,p.2380-2384,5

[73]AngewandteChemie-InternationalEdition,2020,vol.59,p.11010-11019    Angew.Chem.,2020,vol.132,p.11103-11112,10

1821-12-1    18328-11-5 

[1]Fujihara,Tetsuaki;Cong,Cong;Terao,Jun;Tsuji,Yasushi[AdvancedSynthesisandCatalysis,2013,vol.355,#17,p.3420-3424]

[2]Aggarwal,VarinderK.;Noble,Adam;Tyler,JasperL.[AngewandteChemie-InternationalEdition,2022,vol.61,#3][Angew.Chem.,2022,vol.134,#3]

[3]Angle,StevenR.;Arnaiz,DamianO.;Boyce,JamesP.;Frutos,RogelioP.;Louie,MichaelS.;etal.[JournalofOrganicChemistry,1994,vol.59,#21,p.6322-6337]

[4]Salvino,JosephM.;Mervic,Miljenko;Mason,HelenJ.;Kiesow,Terence;Teager,David;Airey,John;Labaudiniere,Richard[JournalofOrganicChemistry,1999,vol.64,#6,p.1823-1830]

[5]Roda,Gabriella;Riva,Sergio;Danieli,Bruno[TetrahedronAsymmetry,1999,vol.10,#20,p.3939-3949]

[6]Kawakami;Kitani;Yuasa;Abe;Moriwaki;Kagoshima;Terasawa;Tahara[EuropeanJournalofMedicinalChemistry,1996,vol.31,#9,p.683-692]

[7]Penn,JohnH.;Liu,Fang[JournalofOrganicChemistry,1994,vol.59,#9,p.2608-2612]

[8]Ellis-Davies,GrahamC.R.;Gilbert,Andrew;Heath,Peter;Lane,JonC.;Warrington,JohnV.;Westover,DavidL.[JournaloftheChemicalSociety.PerkintransactionsII,1984,p.1833-1842]

[9]Fujihara,Tetsuaki;Cong,Cong;Iwai,Tomohiro;Terao,Jun;Tsuji,Yasushi[Synlett,2012,vol.23,#16,p.2389-2392]

[10]Duan,Yitao;Yao,Peiyuan;Chen,Xi;Liu,Xiangtao;Zhang,Rui;Feng,Jinhui;Wu,Qiaqing;Zhu,Dunming[JournalofMolecularCatalysisB:Enzymatic,2015,vol.115,p.1-7]

[11]Shimogaki,Mio;Fujita,Morifumi;Sugimura,Takashi[AngewandteChemie-InternationalEdition,2016,vol.55,#51,p.15797-15801][Angew.Chem.,2016,vol.128,p.16029-16033,5]

[12]Shiely,AmyE.;Slattery,CatherineN.;Ford,Alan;Eccles,KevinS.;Lawrence,SimonE.;Maguire,AnitaR.[OrganicandBiomolecularChemistry,2017,vol.15,#12,p.2609-2628]

[13]Nouaille,Augustin;Pannecoucke,Xavier;Poisson,Thomas;Couve-Bonnaire,Samuel[AdvancedSynthesisandCatalysis,2021,vol.363,#8,p.2140-2147]

18328-11-5    40018-25-5    183129-90-0 

[1]Kawakami;Kitani;Yuasa;Abe;Moriwaki;Kagoshima;Terasawa;Tahara[EuropeanJournalofMedicinalChemistry,1996,vol.31,#9,p.683-692]

75-52-5    18328-11-5    882869-36-5 

[1]Patent:US2006/79562,2006,A1.Locationinpatent:Page/Pagecolumn19

[2]ActaChemicaScandinavica,1999,vol.53,p.792-799

Literature fold

Title: Inversion of stereoselectivity by applying mutants of the hydroxynitrile lyase from Manihot esculenta.

Journal: Chembiochem : a European journal of chemical biology20050401

Title: Conformationally rigid N-acyl-5-alkyl-L-prolyl-pyrrolidines as prolyl oligopeptidase inhibitors.

Journal: Bioorganic & medicinal chemistry20030815

Title: Non-thiol farnesyltransferase inhibitors: structure-activity relationships of aralkylsubstituted benzophenones.

Journal: Archiv der Pharmazie20010201

Related Products of of 18328-11-5
1007-32-5
1007-32-5
1009-14-9
1009-14-9
1199-98-0
1199-98-0
1466-74-6
1466-74-6
1469-83-6
1469-83-6
14721-44-9
14721-44-9
Building Blocks More >
20173-98-2
20173-98-2
1H-Pyrazole, 1-ethenyl-
AA0027QJ | MFCD02823860
202208-73-9
202208-73-9
4-(3-Ethoxyphenyl)benzoic acid
AA00281U | MFCD03426474
202865-57-4
202865-57-4
1-Bromo-2,5-dichloro-3-fluorobenzene
AA0028EX | MFCD00142585
20320-44-9
20320-44-9
2-(Piperidin-1-ylcarbonyl)benzoic acid
AA0028NV | MFCD00443957
203626-46-4
203626-46-4
4,8-Dichloro-2,6-dimethylquinoline
AA0028XS | MFCD00272448
2040-14-4
2040-14-4
2'-Methylpropiophenone
AA00295O | MFCD05663689
204384-26-9
204384-26-9
4-(4-Fluorophenyl)-1h-pyrazole
AA0029E1 | MFCD12131135
20491-92-3
20491-92-3
2,4,6-Trimethoxyphenol
AA0029P2 | MFCD00017159
20532-06-3
20532-06-3
3-(Aminosulfonyl)-4-methoxybenzoic acid
AA0029XY | MFCD06355949
205744-82-7
205744-82-7
2-(4-Chloro-2-nitrophenyl)malondialdehyde
AA002A8A | MFCD00216498
Submit
© 2017 AA BLOCKS, INC. All rights reserved.