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经验公式(希尔记法):
C7H7ClF3NO2
化学文摘社编号:
分子量:
229.58
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
480791
产品名称
(S)-(-)-N-(三氟乙酰基)吡咯烷-2-羰酰氯 溶液, 0.1 M in methylene chloride
InChI
1S/C7H7ClF3NO2/c8-5(13)4-2-1-3-12(4)6(14)7(9,10)11/h4H,1-3H2/t4-/m0/s1
SMILES string
FC(F)(F)C(=O)N1CCC[C@H]1C(Cl)=O
InChI key
NUOYJPPISCCYDH-BYPYZUCNSA-N
optical purity
ee: 95% (GLC)
concentration
0.1 M in methylene chloride
refractive index
n20/D 1.424
density
1.308 g/mL at 25 °C
functional group
acyl chloride
fluoro
storage temp.
2-8°C
Quality Level
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Application
(S)-(−)-N-(Trifluoroacetyl)pyrrolidine-2-carbonyl chloride can be used as a chiral derivatization reagent:
- In the chiral separation of psychoactive, cathinone- and amphetamine-related drugs using GC-MS technique.
- In the estimation of cathinone related drug enantiomers in biological samples like urine and plasma using GC-MS technique.
signalword
Warning
hcodes
Hazard Classifications
Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Central nervous system
存储类别
6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
A validated gas chromatography mass spectrometry method for simultaneous determination of cathinone related drug enantiomers in urine and plasma
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Here we assess the potential functional role of increased aquaporin 9 (APQ9) in astrocytes. Increased AQP9 expression was achieved in primary astrocyte cultures by transfection of a plasmid-containing green fluorescent protein fused to either wild-type or mutated human AQP9. Increased
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Journal of biochemical and biophysical methods, 54(1-3), 103-113 (2003-01-25)
Several important chiral phenethylamine agents such as mexiletine, fenfluramine, amphetamine, methamphetamine and N-n-propylamphetamine show stereoselective disposition in humans and large differences in therapeutic relevance and toxicity. To analyze the enantiomers of chiral amine drugs, stereoselective methods were developed to separate
Simultaneous quantitative determination of synthetic cathinone enantiomers in urine and plasma using GC-NCI-MS
Alremeithi R, et al.
Journal of Analytical Methods in Chemistry, 2018 (2018)
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