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线性分子式:
CF3CH2NH2 · HCl
化学文摘社编号:
分子量:
135.52
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-771-1
Beilstein/REAXYS Number:
3652103
MDL number:
产品名称
2,2,2-三氟乙胺 盐酸盐, 98%
InChI key
ZTUJDPKOHPKRMO-UHFFFAOYSA-N
InChI
1S/C2H4F3N.ClH/c3-2(4,5)1-6;/h1,6H2;1H
SMILES string
Cl.NCC(F)(F)F
assay
98%
mp
220-222 °C (subl.) (lit.)
functional group
amine
fluoro
Quality Level
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Application
2,2,2-三氟乙胺盐酸盐被用于羧酸水溶液的衍生化,生成相应的2,2,2-三氟乙酰胺衍生物。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral
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
Yoshikazu Hattori et al.
Journal of biomolecular NMR, 68(4), 271-279 (2017-08-02)
The preparation of stable isotope-labeled proteins is important for NMR studies, however, it is often hampered in the case of eukaryotic proteins which are not readily expressed in Escherichia coli. Such proteins are often conveniently investigated following post-expression chemical isotope
Quincy LaRon Ford et al.
Journal of chromatography. A, 1145(1-2), 241-245 (2007-02-20)
We report a technique for the rapid, room temperature derivatization of aqueous carboxylic acids to the corresponding 2,2,2-trifluoroethylamide derivative. 3-Ethyl-1-[3-(dimethylamino)propyl]carbodiimide hydrochloride (EDC) and 2,2,2-trifluoroethylamine hydrochloride (TFEA) were added to aqueous samples of several acids of interest in environmental analytical chemistry
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