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33567-53-2 | Methyl 3-(2-Methoxyphenyl)oxirane-2-carboxylate
CAS No: 33567-53-2 Catalog No: AG01F9XJ MDL No:
Product Description
Catalog Number:
AG01F9XJ
Chemical Name:
Methyl 3-(2-Methoxyphenyl)oxirane-2-carboxylate
CAS Number:
33567-53-2
Molecular Formula:
C11H12O4
Molecular Weight:
208.2106
IUPAC Name:
methyl 3-(2-methoxyphenyl)oxirane-2-carboxylate
InChI:
InChI=1S/C11H12O4/c1-13-8-6-4-3-5-7(8)9-10(15-9)11(12)14-2/h3-6,9-10H,1-2H3
InChI Key:
BRZNUGSVQMGEQG-UHFFFAOYSA-N
SMILES:
COC(=O)C1OC1c1ccccc1OC
NSC Number:
110709
Properties
Complexity:
241
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
208.074g/mol
Formal Charge:
0
Heavy Atom Count:
15
Hydrogen Bond Acceptor Count:
4
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
208.213g/mol
Monoisotopic Mass:
208.074g/mol
Rotatable Bond Count:
4
Topological Polar Surface Area:
48.1A^2
Undefined Atom Stereocenter Count:
2
Undefined Bond Stereocenter Count:
0
XLogP3:
1.3
Literature
| Title | Journal |
|---|---|
| Optimization of Serratia marcescens lipase production for enantioselective hydrolysis of 3-phenylglycidic acid ester. | Journal of industrial microbiology & biotechnology 20041201 |
| Highly enantioselective mukaiyama aldol reaction of alpha,alpha-dichloro ketene silyl acetal: an efficient synthesis of a key intermediate for diltiazem. | The Journal of organic chemistry 20030207 |
| A practical procedure for the large-scale preparation of methyl (2R,3S)-3-(4-methoxyphenyl)glycidate, a key intermediate for diltiazem. | The Journal of organic chemistry 20020628 |
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