16503
2-溴-2-丁烯酸甲酯
(cis+trans), ≥95.0% (GC)
别名:
2-溴代巴豆酸甲酯
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线性分子式:
CH3CH=CBrCOOCH3
化学文摘社编号:
分子量:
179.01
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
241-627-1
Beilstein/REAXYS Number:
1700999
MDL number:
Assay:
≥95.0% (GC)
InChI key
DMKWWKUPZZAUQL-UHFFFAOYSA-N
InChI
1S/C5H7BrO2/c1-3-4(6)5(7)8-2/h3H,1-2H3
SMILES string
COC(=O)C(Br)=CC
assay
≥95.0% (GC)
refractive index
n20/D 1.486
bp
178-182 °C (lit.)
density
1.505 g/mL at 20 °C (lit.)
functional group
bromo, ester
storage temp.
2-8°C
Quality Level
General description
Methyl 2-bromo-2-butenoate(Methyl (Z)-2-bromocrotonate) yields (S)-2-bromobutanoic acid by baker′s yeast fermentation. It undergoes biotransformation catalyzed by old yellow enzyme to yield methyl (S)-2-bromobutanoate, a key intermediate for the synthesis of chiral drugs. It is a biannelating reagent which participates in double Michael-additions.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
145.4 °F - closed cup
flash_point_c
63 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
H. Hagiwara et al.
Journal of the Chemical Society. Chemical Communications, 413-413 (1976)
Enoate reductase-mediated preparation of methyl (S)-2-bromobutanoate, a useful key intermediate for the synthesis of chiral active pharmaceutical ingredients.
Brenna E, et al.
Organic Process Research & Development, 16(2), 262-268 (2011)
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