Skip to Content
Merck
All Photos(1)

Key Documents

297984

Sigma-Aldrich

Methyl trans-3-(4-methoxyphenyl)glycidate

97%

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C11H12O4
CAS Number:
Molecular Weight:
208.21
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

Assay

97%

mp

69-71 °C (lit.)

SMILES string

COC(=O)[C@H]1O[C@@H]1c2ccc(OC)cc2

InChI

1S/C11H12O4/c1-13-8-5-3-7(4-6-8)9-10(15-9)11(12)14-2/h3-6,9-10H,1-2H3/t9-,10+/m1/s1

InChI key

CVZUMGUZDAWOGA-ZJUUUORDSA-N

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Y Yamada et al.
International archives of occupational and environmental health, 60(1), 7-14 (1988-01-01)
Forty-nine out of 54 male workers engaged in the production of an epoxy compound, t-methyl-3-phenylglycidate, showed skin symptoms in varying degrees that may be due to the skin-irritative effect of the compound. The exposed workers were also shown to have
Ritsuo Imashiro et al.
The Journal of organic chemistry, 68(3), 974-979 (2003-02-01)
An efficient synthesis of methyl (2R,3S)-3-(4-methoxyphenyl)glycidate (-)-2, a key intermediate for diltiazem (1), has been developed on the basis of the highly enantioselective Mukaiyama aldol reaction of p-anisaldehyde (4a) with alpha,alpha-dichloro ketene silyl acetal 5. Thus, the reaction using a
Occupational contact dermatitis from trans-methyl-3-(4-methoxyphenyl)glycidate.
H Buisson et al.
Contact dermatitis, 25(4), 262-263 (1991-10-01)
Dermatitis from methyl 2,3 epoxy-3-(4-methoxyphenyl)propionate.
E Rudzki et al.
Contact dermatitis, 23(5), 382-382 (1990-11-01)
Li Gao et al.
Journal of industrial microbiology & biotechnology, 31(11), 525-530 (2004-11-19)
Lipase production and cell growth of Serratia marcescens ECU1010 were optimized in shake flasks, with lipase production being enhanced 9.5-fold (4,780 U/l) compared with the initial activity (500 U/l). Optimal carbon and nitrogen sources were Tween-80 and peptone, and the

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service