Home Other Building Blocks Benzyl Glycidyl Ether

Benzyl Glycidyl Ether

CAS No.:
89616-40-0
Catalog Number:
AG01EN61
Molecular Formula:
Molecular Weight:
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Product Description
Catalog Number:
AG01EN61
Chemical Name:
Benzyl Glycidyl Ether
CAS Number:
89616-40-0
MDL Number:
MFCD18911135
IUPAC Name:
2-(phenylmethoxymethyl)oxirane
InChI:
InChI=1S/C10H12O2/c1-2-4-9(5-3-1)6-11-7-10-8-12-10/h1-5,10H,6-8H2
InChI Key:
QNYBOILAKBSWFG-UHFFFAOYSA-N
EC Number:
920-007-0
Properties
Complexity:
130  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
164.084g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
164.204g/mol
Monoisotopic Mass:
164.084g/mol
Rotatable Bond Count:
4  
Topological Polar Surface Area:
21.8A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
1.3  
Literature
Title Journal
Bioresolution of benzyl glycidyl ether using whole cells of Bacillus alcalophilus. Journal of basic microbiology 20120801
Biocatalytic resolution of benzyl glycidyl ether and its derivates by Talaromyces flavus: effect of phenyl ring substituents on enantioselectivity. Biotechnology letters 20120801
Marine fungi Aspergillus sydowii and Trichoderma sp. catalyze the hydrolysis of benzyl glycidyl ether. Marine biotechnology (New York, N.Y.) 20110401
Cloning of an epoxide hydrolase-encoding gene from Aspergillus niger M200, overexpression in E. coli, and modification of activity and enantioselectivity of the enzyme by protein engineering. Journal of biotechnology 20071015
Purification and characterisation of a novel enantioselective epoxide hydrolase from Aspergillus niger M200. Biochimica et biophysica acta 20060201
Novel microbial epoxide hydrolases for biohydrolysis of glycidyl derivatives. Journal of biotechnology 20051206
Synthesis of 4-deoxy-L-(and D-)hexoses from chiral noncarbohydrate building blocks. The Journal of organic chemistry 20041015
Practical, asymmetric synthesis of 16-hydroxyeicosa-5(Z),8(Z), 11(Z),14(Z)-tetraenoic acid (16-HETE), an endogenous inhibitor of neutrophil activity. Bioorganic & medicinal chemistry letters 20031103
Discovery and characterization of the potent, selective and orally bioavailable MMP inhibitor ABT-770. Bioorganic & medicinal chemistry letters 20010618
Properties