686301
(S)-4-溴-α-甲基苯甲醇
95%
别名:
(S)-1-(4-溴苯基)乙醇, (S)-4′-溴-1-苯基乙醇
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关于此项目
线性分子式:
BrC6H4CH(CH3)OH
化学文摘社编号:
分子量:
201.06
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352101
MDL number:
产品名称
(S)-4-溴-α-甲基苯甲醇, 95%
InChI
1S/C8H9BrO/c1-6(10)7-2-4-8(9)5-3-7/h2-6,10H,1H3/t6-/m0/s1
SMILES string
C[C@H](O)c1ccc(Br)cc1
InChI key
XTDTYSBVMBQIBT-LURJTMIESA-N
assay
95%
form
liquid
optical activity
[α]20/D -38.0°, c = 1 in chloroform
refractive index
n20/D 1.570
density
1.322 g/mL at 25 °C
functional group
bromo
hydroxyl
Quality Level
signalword
Warning
Hazard Classifications
Acute Tox. 4 Oral - 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
>230.0 °F
flash_point_c
> 110 °C
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Xiao-Hong Chen et al.
PloS one, 9(4), e94543-e94543 (2014-04-18)
A novel carbonyl reductase (AcCR) catalyzing the asymmetric reduction of ketones to enantiopure alcohols with anti-Prelog stereoselectivity was found in Acetobacter sp. CCTCC M209061 and enriched 27.5-fold with an overall yield of 0.4% by purification. The enzyme showed a homotetrameric
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