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Merck
CN

720151

(S)-2-(2-溴苯基)-4-异丙基-5,5-二甲基-4,5-二氢噁唑

96%

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关于此项目

经验公式(希尔记法):
C14H18BrNO
分子量:
296.20
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
Assay:
96%
Form:
liquid
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assay

96%

form

liquid

optical activity

[α]22/D −41.0°, c = 0.5 in chloroform

refractive index

n20/D 1.541

density

1.247 g/mL at 25 °C

functional group

bromo, ether

SMILES string

CC1(C)[C@H](C(C)C)N=C(C2=CC=CC=C2Br)O1

InChI

1S/C14H18BrNO/c1-9(2)12-14(3,4)17-13(16-12)10-7-5-6-8-11(10)15/h5-9,12H,1-4H3/t12-/m0/s1

InChI key

SJKCCGPXYWNYGX-LBPRGKRZSA-N

Application

(S)-2-(2-Bromophenyl)-4-isopropyl-5,5-dimethyl-4,5-dihydrooxazole can be used as a key intermediate for the preparation of (S)-5,5-(dimethyl)-i-Pr-PHOX, a chiral ligand employed in the palladium-catalyzed asymmetric transformations.


存储类别

10 - Combustible liquids

wgk

nwg

flash_point_f

>230.0 °F - closed cup

flash_point_c

> 110 °C - closed cup

法规信息

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分析证书(COA)

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Design, Synthesis, and Applications of Potential Substitutes of t-Bu-Phosphinooxazoline in Pd-Catalyzed Asymmetric Transformations and Their Use for the Improvement of the Enantioselectivity in the Pd-Catalyzed Allylation Reaction of Fluorinated Allyl Enol Carbonates
Belanger E, et al.
The Journal of Organic Chemistry, 77(1), 317-331 (2012)



全球贸易项目编号

货号GTIN
720151-1G04061826734865