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6971-51-3,MFCD00004637
Catalog No.:AA003JKL

6971-51-3 | 3-Methoxybenzyl alcohol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%
in stock  
$6.00   $4.00
- +
10g
98%
in stock  
$7.00   $5.00
- +
25g
98%
in stock  
$14.00   $10.00
- +
100g
98%
in stock  
$52.00   $36.00
- +
  • 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:
AA003JKL
Chemical Name:
3-Methoxybenzyl alcohol
CAS Number:
6971-51-3
Molecular Formula:
C8H10O2
Molecular Weight:
138.1638
MDL Number:
MFCD00004637
SMILES:
OCc1cccc(c1)OC
NSC Number:
66559
Properties
Properties
 
BP:
247.4°C at 760 mmHg  
Form:
Liquid  
MP:
30°C  
Refractive Index:
n20/D 1.540(lit.)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
93.3  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
2  
XLogP3:
1.2  

Upstream Synthesis Route

[1]Patent:CN105859654,2016,A,

[1]ChemMedChem,2011,vol.6,#12,p.2273-2286

[1]Patent:WO2016/16238,2016,A1,.Locationinpatent:Page/Pagecolumn126-127

[2]OrganicProcessResearchandDevelopment,2016,vol.20,#2,p.568-573

[3]BioorganicandMedicinalChemistry,2008,vol.16,#19,p.8889-8895

[4]JournalofOrganicChemistry,1998,vol.63,#25,p.9565-9568

[5]AustralianJournalofChemistry,1992,vol.45,#1,p.71-97

[6]JournalofChemicalResearch,2004,#3,p.232-233

[7]JournalofOrganicChemistry,1981,vol.46,#11,p.2394-2398

[8]ChemicalandPharmaceuticalBulletin,1993,vol.41,#11,p.2003-2006

[9]AustralianJournalofChemistry,1984,vol.37,#4,p.893-901

[10]JournaloftheAmericanChemicalSociety,1942,vol.64,p.2031,2033

[11]JournaloftheChemicalSociety,1935,p.1533,1543

[12]JournaloftheChemicalSociety,1942,p.684,687

[13]JustusLiebigsAnnalenderChemie,1912,vol.391,p.44

[14]JournaloftheChemicalSociety[Section]B:PhysicalOrganic,1968,p.1529-1533

[15]BulletindelaSocieteChimiquedeFrance,1973,p.3433-3436

[16]Heterocycles,1997,vol.45,#11,p.2137-2157

[17]BioorganicandMedicinalChemistryLetters,2001,vol.11,#16,p.2205-2208

[18]EuropeanJournalofMedicinalChemistry,2002,vol.37,#4,p.339-347

[19]SyntheticCommunications,2003,vol.33,#10,p.1727-1732

[20]OrganicLetters,2013,vol.15,#1,p.108-111

[21]OrganicandBiomolecularChemistry,2013,vol.11,#24,p.4016-4024

[22]BioorganicandMedicinalChemistry,2015,vol.23,#4,p.657-667

[23]Patent:CN105859654,2016,A,.Locationinpatent:Paragraph0009;0015-0016

[24]Patent:US4055574,1977,A,

[25]Patent:US3947520,1976,A,

[1]ChemSusChem,2016,vol.9,#1,p.67-74

[1]ChemCatChem,2018,vol.10,#9,p.1993-1997

Downstream Synthesis Route

[1]Patent:WO2016/16238,2016,A1.Locationinpatent:Page/Pagecolumn126-127

[2]OrganicProcessResearchandDevelopment,2016,vol.20,p.568-573

[3]BioorganicandMedicinalChemistry,2008,vol.16,p.8889-8895

[4]JournalofOrganicChemistry,1998,vol.63,p.9565-9568

[5]AustralianJournalofChemistry,1992,vol.45,p.71-97

[6]JournalofChemicalResearch,2004,p.232-233

[7]Synlett,2019,vol.30,p.943-946

[8]JournalofOrganicChemistry,1981,vol.46,p.2394-2398

[9]ChemicalandPharmaceuticalBulletin,1993,vol.41,p.2003-2006

[10]AustralianJournalofChemistry,1984,vol.37,p.893-901

[11]JournaloftheAmericanChemicalSociety,1942,vol.64,p.2031,2033

[12]JournaloftheChemicalSociety,1935,p.1533,1543

[13]JustusLiebigsAnnalenderChemie,1912,vol.391,p.44

[14]JournaloftheChemicalSocietyB:PhysicalOrganic,1968,p.1529-1533

[15]BulletindelaSocieteChimiquedeFrance,1973,p.3433-3436

[16]Heterocycles,1997,vol.45,p.2137-2157

[17]BioorganicandMedicinalChemistryLetters,2001,vol.11,p.2205-2208

[18]EuropeanJournalofMedicinalChemistry,2002,vol.37,p.339-347

[19]SyntheticCommunications,2003,vol.33,p.1727-1732

[20]OrganicLetters,2013,vol.15,p.108-111

[21]OrganicandBiomolecularChemistry,2013,vol.11,p.4016-4024

[22]BioorganicandMedicinalChemistry,2015,vol.23,p.657-667

[23]Patent:CN105859654,2016,A.Locationinpatent:Paragraph0009;0015-0016

[24]Patent:US4055574,1977,A

[25]Patent:US3947520,1976,A

[26]TetrahedronLetters,2020

[1]Wang,Hu;Li,Li;Bai,Xing-Feng;Shang,Jun-Yan;Yang,Ke-Fang;Xu,Li-Wen[AdvancedSynthesisandCatalysis,2013,vol.355,#2-3,p.341-347]

[2]Huang,Jian-Lin;Dai,Xi-Jie;Li,Chao-Jun[EuropeanJournalofOrganicChemistry,2013,#29,p.6496-6500]

[3]Dai,Xi-Jie;Li,Chao-Jun[JournaloftheAmericanChemicalSociety,2016,vol.138,#16,p.5433-5440]

[4]Wenderetal.[JournaloftheAmericanChemicalSociety,1952,vol.74,p.4079,4082]

[5]Gómez,Cecilia;Maciá,Beatriz;Lillo,VictorJ.;Yus,Miguel[Tetrahedron,2006,vol.62,#42,p.9832-9839]

[1]Kaiser,Florian;Schwink,Lothar;Velder,Janna;Schmalz,Hans-Guenther[JournalofOrganicChemistry,2002,vol.67,#26,p.9248-9256]

[2]Trost,BarryM.;Rivers,GordonT.;Gold,JeffreyM.[JournalofOrganicChemistry,1980,vol.45,#10,p.1835-1838]

[3]Dodsworth,DavidJ.;Calcagno,Maria-Pia;Ehrmann,E.Ursula;Devadas,Bhatt;Sammes,PeterG.[JournaloftheChemicalSociety.PerkintransactionsI,1981,p.2120-2124]

[4]Orito,Kazuhiko;Miyazawa,Mamoru;Suginome,Hiroshi[Tetrahedron,1995,vol.51,#9,p.2489-2496]

[1]BulletinoftheChemicalSocietyofJapan,1988,vol.61,p.1221-1224

[1]BulletinoftheChemicalSocietyofJapan,1991,vol.64,p.2295-2297

Literature

Title: Characterization of four Rhodococcus alcohol dehydrogenase genes responsible for the oxidation of aromatic alcohols.

Journal: Applied microbiology and biotechnology 20060801

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