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Methyl-trans-3-(4-methoxyphenyl)glycidat
97%
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About This Item
Empirische Formel (Hill-System):
C11H12O4
CAS-Nummer:
Molekulargewicht:
208.21
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12162002
PubChem Substanz-ID:
NACRES:
NA.23
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Assay
97%
mp (Schmelzpunkt)
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
InChIKey
CVZUMGUZDAWOGA-ZJUUUORDSA-N
Signalwort
Warning
H-Sätze
Gefahreneinstufungen
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Zielorgane
Respiratory system
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
dust mask type N95 (US), Eyeshields, Gloves
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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
Leukocytosis and low serum IgA in workers exposed to the epoxy compound, t-methyl-3-phenylglycidate.
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
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
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