Home Other Building Blocks 7314-44-5
7314-44-5,MFCD00004614
Catalog No.:AA003B26

7314-44-5 | 2,4-Dimethoxybenzyl alcohol

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5g
98%
in stock  
$13.00   $9.00
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10g
98%
in stock  
$16.00   $11.00
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25g
98%
in stock  
$38.00   $27.00
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100g
98%
in stock  
$77.00   $54.00
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500g
98%
in stock  
$384.00   $269.00
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  • 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:
AA003B26
Chemical Name:
2,4-Dimethoxybenzyl alcohol
CAS Number:
7314-44-5
Molecular Formula:
C9H12O3
Molecular Weight:
168.1898
MDL Number:
MFCD00004614
SMILES:
COc1cc(OC)ccc1CO
Properties
Properties
 
BP:
316.7°C at 760 mmHg  
Form:
Solid  
MP:
38-40 °C(lit.)  
Refractive Index:
1.545-1.548  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
127  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
3  
Undefined Atom Stereocenter Count:
1  
XLogP3:
1.5  

Upstream Synthesis Route

[1]SyntheticCommunications,2001,vol.31,#17,p.2719-2725

[2]OrganicLetters,2015,vol.17,#3,p.434-437

[3]TetrahedronLetters,1992,vol.33,#37,p.5417-5418

[4]IndianJournalofChemistry,SectionB:OrganicChemistryIncludingMedicinalChemistry,1994,vol.33,#2,p.182-183

[5]TetrahedronLetters,1994,vol.35,#1,p.65-68

[6]SyntheticCommunications,1995,vol.25,#7,p.941-945

[7]SyntheticCommunications,2014,vol.44,#2,p.280-288

[8]JournalofPhysicalOrganicChemistry,2006,vol.19,#3,p.214-218

[9]AsianJournalofChemistry,2010,vol.22,#9,p.6761-6764

[10]TetrahedronLetters,1990,vol.31,#52,p.7663-7664

[11]SyntheticCommunications,2004,vol.34,#4,p.643-650

[12]Molecules,2006,vol.11,#5,p.365-369

[13]EuropeanJournalofMedicinalChemistry,2012,vol.55,p.125-136

[14]AppliedOrganometallicChemistry,2015,vol.29,#1,p.45-49

[15]ResearchonChemicalIntermediates,2015,vol.41,#12,p.9281-9294

[16]ChemSusChem,2014,vol.7,#9,p.2684-2689

[17]EuropeanJournalofMedicinalChemistry,2018,vol.143,p.1345-1360

[18]NewJournalofChemistry,2018,vol.42,#19,p.15572-15577

[1]TetrahedronLetters,2003,vol.44,#16,p.3427-3428

[2]Synthesis,2011,#9,p.1375-1382

[1]JournalofOrganicChemistry,2006,vol.71,#8,p.3149-3153

[1]OrganicandBiomolecularChemistry,2018,vol.16,#2,p.274-284

[1]Synthesis,2011,#9,p.1375-1382

Downstream Synthesis Route

[1]JournaloftheChemicalSociety.Chemicalcommunications,1992,p.274-275

[2]JournalofFluorineChemistry,1991,vol.54,p.268

[1]Terauchi,Hideo;Tanitame,Akihiko;Tada,Keiko;Nakamura,Keiji;Seto,Yasuhiro;Nishikawa,Yoshinori[JournalofMedicinalChemistry,1997,vol.40,#3,p.313-321]

[2]Terauchi,Hideo;Tanitame,Akihiko;Tada,Keiko;Nishikawa,Yoshinori[Heterocycles,1996,vol.43,#8,p.1719-1734]

3195-78-6    7314-44-5   
<i>N</i>-1-(2,4-dimethoxy-benzyloxy)-ethyl-<i>N</i>-methyl-acetamide 

[1]JournalofOrganicChemistry,2004,vol.69,p.584-586

[1]JournaloftheAmericanChemicalSociety,2001,vol.123,p.3623-3629

[1]BioorganicandMedicinalChemistry,2006,vol.14,p.7539-7550

[2]JournaloftheAmericanChemicalSociety,2003,vol.125,p.1575-1586

[3]Synthesis,2001,p.1086-1092

[4]TetrahedronLetters,1998,vol.39,p.7865-7868

[5]JournalofMedicinalChemistry,2010,vol.53,p.6071-6078

Literature

Title: Aryl phosphoramidates of 5-phospho erythronohydroxamic acid, a new class of potent trypanocidal compounds.

Journal: Journal of medicinal chemistry 20100826

Title: Synthesis and biological evaluation of phosphate prodrugs of 4-phospho-D-erythronohydroxamic acid, an inhibitor of 6-phosphogluconate dehydrogenase.

Journal: ChemMedChem 20070813

Title: Fluorous reagents and scavengers versus solid-supported reagents and scavengers, a reaction rate and kinetic comparison.

Journal: Molecular diversity 20050101

Title: Marie Couturier, et al. Characterization of a new aryl-alcohol oxidase secreted by the phytopathogenic fungus Ustilago maydis. Appl Microbiol Biotechnol. 2016 Jan;100(2):697-706.

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