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Merck
CN

667005

Sigma-Aldrich

(R)-(+)-3,3,3-三氟-1,2-环氧丙烷

97%

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别名:
(R)-(+)-2-三氟甲基环氧乙烷
经验公式(希尔记法):
C3H3F3O
分子量:
112.05
MDL编号:
UNSPSC代码:
12352005
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

97%

折射率

n20/D <1.300

bp

25-32 °C

密度

1.294 g/mL at 25 °C

储存温度

2-8°C

SMILES字符串

FC(F)(F)[C@H]1CO1

InChI

1S/C3H3F3O/c4-3(5,6)2-1-7-2/h2H,1H2/t2-/m1/s1

InChI key

AQZRARFZZMGLHL-UWTATZPHSA-N

应用

(R)-(+)-3,3,3-Trifluoro-1,2-epoxypropane can be used as a substrate to synthesize:
  • Substituted trifluoro amino propanols, which are found to be potent inhibitors of cholesteryl ester transfer protein.
  • (2R) Trifluoro-(methoxybenzyloxy)-propanol (chiral glycol) by reacting with 4-methoxybenzyl alcohol in the presence of NaH. Chiral glycol intermediate is further utilized for the preparation of trifluoromethyl glycol carbamates as potential monoacylglycerol lipase (MAGL) inhibitors.

象形图

Flame

警示用语:

Danger

危险声明

预防措施声明

危险分类

Flam. Liq. 1

WGK

WGK 3

闪点(°F)

-14.8 °F

闪点(°C)

-26 °C

个人防护装备

Eyeshields, Faceshields, Gloves

法规信息

危险化学品

分析证书(COA)

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Discovery of trifluoromethyl glycol carbamates as potent and selective covalent monoacylglycerol lipase (MAGL) inhibitors for treatment of neuroinflammation
McAllister LA, et al.
Journal of Medicinal Chemistry, 61(7), 3008-3026 (2018)
Discovery of a simple picomolar inhibitor of cholesteryl ester transfer protein
Reinhard EJ, et al.
Journal of Medicinal Chemistry, 46(11), 2152-2168 (2003)
Emily J Reinhard et al.
Journal of medicinal chemistry, 46(11), 2152-2168 (2003-05-16)
A novel series of substituted N-[3-(1,1,2,2-tetrafluoroethoxy)benzyl]-N-(3-phenoxyphenyl)-trifluoro-3-amino-2-propanols is described which potently and reversibly inhibit cholesteryl ester transfer protein (CETP). Starting from the initial lead 1, various substituents were introduced into the 3-phenoxyaniline group to optimize the relative activity for inhibition of

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