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297984

Sigma-Aldrich

Methyl trans-3-(4-methoxyphenyl)glycidate

97%

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About This Item

Empirical Formula (Hill Notation):
C11H12O4
CAS Number:
42245-42-1
Molecular Weight:
208.21
EC Number:
255-735-1
MDL number:
MFCD00012316
UNSPSC Code:
12162002
PubChem Substance ID:
24857951
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
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

297984-25G:
297984-5G:
297984-1G:
297984-BULK:
297984-VAR:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Dermatitis from methyl 2,3 epoxy-3-(4-methoxyphenyl)propionate.
E Rudzki et al.
Contact dermatitis, 23(5), 382-382 (1990-11-01)
Occupational contact dermatitis from trans-methyl-3-(4-methoxyphenyl)glycidate.
H Buisson et al.
Contact dermatitis, 25(4), 262-263 (1991-10-01)
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
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
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
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