667005
(R)-(+)-3,3,3-Trifluoro-1,2-epoxypropane
97%
동의어(들):
(R)-(+)-2-(Trifluoromethyl)oxirane
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About This Item
실험식(Hill 표기법):
C3H3F3O
CAS Number:
Molecular Weight:
112.05
MDL number:
UNSPSC 코드:
12352005
PubChem Substance ID:
NACRES:
NA.22
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추천 제품
Quality Level
분석
97%
refractive index
n20/D <1.300
bp
25-32 °C
density
1.294 g/mL at 25 °C
작용기
ether
fluoro
저장 온도
2-8°C
SMILES string
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
1 of 4
이 품목 | L0551000 | 1362602 | BP501 |
---|---|---|---|
technique(s) HPLC: suitable, gas chromatography (GC): suitable | technique(s) - | technique(s) - | technique(s) - |
format neat | format neat | format neat | format neat |
Quality Level 300 | Quality Level - | Quality Level - | Quality Level - |
grade certified reference material, pharmaceutical secondary standard | grade pharmaceutical primary standard | grade pharmaceutical primary standard | grade pharmaceutical primary standard |
storage temp. 2-8°C | storage temp. - | storage temp. - | storage temp. 2-8°C |
packaging pkg of 500 mg | packaging - | packaging - | packaging - |
애플리케이션
(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.[1]
- (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.[2]
신호어
Danger
유해 및 위험 성명서
예방조치 성명서
Hazard Classifications
Flam. Liq. 1
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
-14.8 °F
Flash Point (°C)
-26 °C
개인 보호 장비
Eyeshields, Faceshields, Gloves
Fouad Fadhil Al-Qaim et al.
Journal of environmental sciences (China), 74, 134-146 (2018-10-21)
Prazosin (PRZ) and levonorgestrel (LNG) are widely used as an anti-disease drugs due to their biological activity in the human body. The frequent detection of these compounds in water samples requires alternative technologies for the removal of both compounds. After
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