338419
(R)-(+)-3-氯-1-苯基-1-丙醇
98%
别名:
α-(2-氯乙基)苄醇, (R)-(+)-α-(2-氯乙基)苄醇, (R)-(+)-3-氯-1-苯丙醇
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关于此项目
线性分子式:
ClCH2CH2CH(C6H5)OH
化学文摘社编号:
分子量:
170.64
UNSPSC Code:
12352101
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5250766
产品名称
(R)-(+)-3-氯-1-苯基-1-丙醇, 98%
InChI
1S/C9H11ClO/c10-7-6-9(11)8-4-2-1-3-5-8/h1-5,9,11H,6-7H2/t9-/m1/s1
SMILES string
O[C@H](CCCl)c1ccccc1
InChI key
JZFUHAGLMZWKTF-SECBINFHSA-N
assay
98%
form
solid
optical activity
[α]24/D +26°, c = 1 in chloroform
optical purity
ee: 99% (GLC)
mp
58-60 °C (lit.)
Application
(R)-(+)-3-Chloro-1-phenyl-1-propanol may be used as a building block in the synthesis of antidepressants such as (R)- and (S)-tomoxetine, fluoxetine and nisoxetine. It may also be used in the synthesis of biologically active 2-substituted chromans such as tephrowatsin E.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
An efficient route to enantiomerically pure antidepressants: tomoxetine, nisoxetine and fluoxetine.
Schneider MP and Goergens U.
Tetrahedron Asymmetry, 3(4), 525-528 (1992)
A stereocontrolled route to 2-substituted chromans.
Hodgetts KJ.
Tetrahedron Letters, 41(44), 8655-8659 (2000)
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