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线性分子式:
BrCH2CH(CH3)CH2OH
化学文摘社编号:
分子量:
153.02
UNSPSC Code:
12352101
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3600269
产品名称
(R)-(-)-3-溴-2-甲基-1-丙醇, 97%
InChI
1S/C4H9BrO/c1-4(2-5)3-6/h4,6H,2-3H2,1H3/t4-/m0/s1
SMILES string
C[C@H](CO)CBr
InChI key
KIBOHRIGZMLNNS-BYPYZUCNSA-N
assay
97%
form
liquid
optical activity
[α]25/D −6.6°, c = 2 in chloroform
refractive index
n20/D 1.484 (lit.)
bp
73-74 °C/9 mmHg (lit.)
density
1.461 g/mL at 20 °C (lit.)
functional group
bromo
hydroxyl
Quality Level
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Application
(R)-(−)-3-溴-2-甲基-1-丙醇作为起始原料用于埃坡霉素 C 和比司酰胺 A 的全合成。也可作为同手性多孔分子网络的结构改性剂。
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
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Multi?step application of immobilized reagents and scavengers: a total synthesis of epothilone C.
Storer R I, et al.
Chemistry?A European Journal , 10(10), 2529-2547 (2004)
Enantioselective total synthesis of bistramide A.
Crimmins M T and DeBaillie A C
Journal of the American Chemical Society, 128(15), 4936-4937 (2006)
Control and induction of surface-confined homochiral porous molecular networks.
Tahara K, et al.
Nature Chemistry, 3(9), 714-719 (2011)
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