+1 858-523-8231
Login | Register
AA Blocks, Building Blocks, Catalysts, Inhibitors
Login | Register
Home Carboxes 3609-53-8
3609-53-8,MFCD00216474
Catalog No.:AA00354E

3609-53-8 | Methyl 4-acetylbenzoate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$9.00   $7.00
- +
5g
98%
in stock  
$12.00   $8.00
- +
10g
98%
in stock  
$15.00   $11.00
- +
25g
98%
in stock  
$35.00   $25.00
- +
100g
98%
in stock  
$138.00   $96.00
- +
500g
98%
in stock  
$484.00   $339.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00354E
Chemical Name:
Methyl 4-acetylbenzoate
CAS Number:
3609-53-8
Molecular Formula:
C10H10O3
Molecular Weight:
178.1846
MDL Number:
MFCD00216474
SMILES:
COC(=O)c1ccc(cc1)C(=O)C
NSC Number:
49140
Properties
Properties
 
BP:
295.6°C at 760 mmHg  
Form:
Solid  
MP:
93-96 °C(lit.)  
Refractive Index:
1.5190 (estimate)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
202  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
3  
Rotatable Bond Count:
3  
XLogP3:
1.9  

Upstream Synthesis Route

[1]JournalofMedicinalChemistry,2012,vol.55,#6,p.2899-2903

[2]JournalofOrganicChemistry,2015,vol.80,#14,p.7212-7218

[1]JournaloftheAmericanChemicalSociety,1959,vol.81,p.257,259

[2]JournaloftheAmericanChemicalSociety,1959,vol.81,p.257,259

[1]JournaloftheAmericanChemicalSociety,2000,vol.122,#39,p.9361-9366

[2]Patent:WO2006/78698,2006,A1,.Locationinpatent:Page/Pagecolumn64

[3]Patent:US2012/196869,2012,A1,.Locationinpatent:Paragraph0467;0468;0469

[4]InorganicChemistry,2018,vol.57,#1,p.120-128

[5]Patent:WO2008/33745,2008,A2,.Locationinpatent:Page/Pagecolumn70-71

[6]Patent:WO2008/33747,2008,A2,.Locationinpatent:Page/Pagecolumn255

[7]Patent:EP2210891,2010,A1,.Locationinpatent:Page/Pagecolumn19

[8]JournalofMedicinalChemistry,2012,vol.55,#6,p.2899-2903

[9]Patent:WO2015/89327,2015,A1,.Locationinpatent:Paragraph0414

[10]Patent:US6525042,2003,B1,

[11]Patent:EP1104754,2001,A1,

[12]Patent:EP1577302,2005,A1,.Locationinpatent:Page/Pagecolumn109

[13]Patent:WO2007/6547,2007,A1,.Locationinpatent:Page/Pagecolumn43-45

[14]Patent:US2009/23748,2009,A1,.Locationinpatent:Page/Pagecolumn24-25

[15]Patent:WO2010/34788,2010,A1,.Locationinpatent:Page/Pagecolumn38

[16]Patent:WO2010/34789,2010,A1,.Locationinpatent:Page/Pagecolumn33

[17]JournalofMedicinalChemistry,1987,vol.30,#8,p.1497-1502

[18]Patent:WO2006/17124,2006,A2,.Locationinpatent:Page/Pagecolumn66

[19]Patent:EP1975149,2008,A1,.Locationinpatent:Page/Pagecolumn64

[20]Patent:US2004/248949,2004,A1,.Locationinpatent:Page35-36

[21]BioorganicandMedicinalChemistry,2010,vol.18,#6,p.2317-2326

[22]Patent:EP2172462,2010,A1,.Locationinpatent:Page/Pagecolumn87

[23]Patent:WO2006/28970,2006,A1,.Locationinpatent:Page/Pagecolumn68-69

[24]Patent:US2011/189794,2011,A1,

[25]Patent:EP2353613,2011,A1,

[26]JournalofMedicinalChemistry,2015,vol.58,#15,p.6058-6080

[27]OrganicLetters,2017,vol.19,#8,p.1994-1997

[28]OrganicLetters,2018,vol.20,#8,p.2257-2260

[29]ChemicalCommunications(Cambridge,UnitedKingdom),2018,vol.54,#86,p.12182-12185

[1]Patent:WO2004/91610,2004,A1,.Locationinpatent:Page/Pagecolumn67

[1]OrganicLetters,2012,vol.14,#9,p.2414-2417

[2]OrganicLetters,2016,vol.18,#4,p.784-787

Downstream Synthesis Route

[1]Tavares;Penna;Amaral[BollettinoChimicoFarmaceutico,1997,vol.136,#3,p.244-249]

[2]CurrentPatentAssignee:CENTRENATIONALDELARECHERCHESCIENTIFIQUE;CENTREINTERNATIONALDERECHERCHEAUXFRONTIERESDELACHIMIE;UNIVERSITYOFPARISSACLAY;UNIVERSITYOFSTRASBOURG;NATIONALINSTITUTEOFHEALTHANDMEDICALRESEARCH-WO2018/11376,2018,A1Locationinpatent:Page/Pagecolumn44

[3]Tavares;Chiste;Santos;Penna[BollettinoChimicoFarmaceutico,1999,vol.138,#8,p.432-436]

[4]CurrentPatentAssignee:DAIICHISANKYOCOMPANY,LIMITED-EP1577302,2005,A1Locationinpatent:Page/Pagecolumn108

[5]CurrentPatentAssignee:NOVARTISAG;Novartis(w/oSandoz)-WO2015/48507,2015,A1Locationinpatent:Paragraph0154

[6]CurrentPatentAssignee:HALLYMUNIVERSITY;EWHAWOMANSUNIVERSITY-KR2021/89017,2021,ALocationinpatent:Paragraph0088;0090-0092;0094-0096

[7]CurrentPatentAssignee:UNIVERSITYOFWASHINGTON-WO2020/123855,2020,A1Locationinpatent:Page/Pagecolumn36

[8]Meyer,R.[JustusLiebigsAnnalenderChemie,1883,vol.219,p.253]

[9]Masunari,Andrea;Tavares,LeobertoCosta[BioorganicandMedicinalChemistry,2007,vol.15,#12,p.4229-4236]

[10]Locationinpatent:experimentalpartJorge,SalomaoDoria;Masunari,Andrea;Rangel-Yagui,CarlotaOliveira;Pasqualoto,KerlyFernandaMesquita;Tavares,LeobertoCosta[BioorganicandMedicinalChemistry,2009,vol.17,#8,p.3028-3036]

[11]Locationinpatent:experimentalpartNakamura,Ryota;Obora,Yasushi;Ishii,Yasutaka[AdvancedSynthesisandCatalysis,2009,vol.351,#10,p.1677-1684]

[12]Hou,Zengye;Nakanishi,Isao;Kinoshita,Takayoshi;Takei,Yoshinori;Yasue,Misato;Misu,Ryosuke;Suzuki,Yamato;Nakamura,Shinya;Kure,Tatsuhide;Ohno,Hiroaki;Murata,Katsumi;Kitaura,Kazuo;Hirasawa,Akira;Tsujimoto,Gozoh;Oishi,Shinya;Fujii,Nobutaka[JournalofMedicinalChemistry,2012,vol.55,#6,p.2899-2903]

[13]CurrentPatentAssignee:CHINAPHARMACEUTICALUNIVERSITY;YAOKANGZHONGTUOJIANGSUPHARMACEUTICALTECH-CN112321513,2021,ALocationinpatent:Paragraph0120-0125

[1]Synthesis,2017,vol.49,p.4007-4016

[2]OrganicLetters,2017,vol.19,p.5593-5596

[3]TetrahedronLetters,2010,vol.51,p.2063-2066

[4]ChemCatChem,2013,vol.5,p.126-129

[5]JournaloftheAmericanChemicalSociety,1946,vol.68,p.674

[1]TetrahedronLetters,2008,vol.49,p.110-113

[2]Synlett,2012,p.433-437

[3]Patent:US5019298,1991,A

[4]TetrahedronLetters,2012,vol.53,p.3686-3688

[5]Tetrahedron,2013,vol.69,p.6399-6403

[6]Chemistry-AnAsianJournal,2010,vol.5,p.1687-1691

[7]EuropeanJournalofOrganicChemistry,2013,p.5439-5444

[8]Tetrahedron,2014,vol.70,p.2088-2095

[9]Chemistry-AEuropeanJournal,2014,vol.20,p.4242-4245

[10]ChemicalCommunications,2007,p.760-762

[11]AppliedOrganometallicChemistry,2011,vol.25,p.748-752

[12]JournaloftheAmericanChemicalSociety,2016,vol.138,p.8809-8814

[13]JournalofOrganicChemistry,2020,vol.85,p.2242-2249

[14]AdvancedSynthesisandCatalysis,2012,vol.354,p.217-222

[15]Patent:WO2013/75083,2013,A1.Locationinpatent:Paragraph00219

[16]Patent:US9206128,2015,B2.Locationinpatent:Page/Pagecolumn122;123

[17]TetrahedronLetters,1982,vol.23,p.4585-4588

[18]EuropeanJournalofOrganicChemistry,2019,vol.2019,p.995-998

[19]Chemistry-AEuropeanJournal,2018,vol.24,p.12259-12263

[20]AngewandteChemie-InternationalEdition,2016,vol.55,p.11806-11809    Angew.Chem.,2016,vol.128,p.11984-11988,5

[21]Patent:CN106146401,2016,A.Locationinpatent:Paragraph0134;0135

[22]JournaloftheAmericanChemicalSociety,1946,vol.68,p.674

[23]JournalofOrganicChemistry,1959,vol.24,p.549

[24]AngewandteChemie-InternationalEdition,2013,vol.52,p.5120-5124    Angew.Chem.,2013,vol.125,p.5224-5228

[25]JournaloftheAmericanChemicalSociety,2016,vol.138,p.6940-6943

[26]Patent:WO2017/142883,2017,A1.Locationinpatent:Paragraph0179-0180

[27]OrganicandBiomolecularChemistry,2019,vol.17,p.4230-4233

[28]Chem,2019,vol.5,p.1552-1566

[29]AngewandteChemie-InternationalEdition,2019,vol.58,p.17567-17571    Angew.Chem.,2019,vol.131,p.17731-17735,5

[30]ChemicalCommunications,2020,vol.56,p.1203-1206

[1]TetrahedronLetters,1992,vol.33,p.5499-5502

[1]ChemistryLetters,1993,p.925-928

Literature

Title: Metal-free carbon-carbon bond-forming reductive coupling between boronic acids and tosylhydrazones.

Journal: Nature chemistry 20090901

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Related Products of 3609-53-8
119838-61-8

119838-61-8

 120-61-6

120-61-6

 129488-73-9

129488-73-9

 136333-97-6

136333-97-6

 13756-42-8

13756-42-8

 143726-85-6

143726-85-6
Building Blocks
More >
Tags:3609-53-8 Molecular Formula|3609-53-8 MDL|3609-53-8 SMILES|3609-53-8 Methyl 4-acetylbenzoate |Organic_Building_Blocks