224936
4-(三氟甲基)苯胺
99%
别名:
α,α,α-三氟对甲苯胺, 4-氨基三氟甲苯
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关于此项目
线性分子式:
CF3C6H4NH2
化学文摘社编号:
分子量:
161.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-236-5
Beilstein/REAXYS Number:
1564853
MDL number:
Assay:
99%
Form:
liquid
InChI key
ODGIMMLDVSWADK-UHFFFAOYSA-N
InChI
1S/C7H6F3N/c8-7(9,10)5-1-3-6(11)4-2-5/h1-4H,11H2
SMILES string
Nc1ccc(cc1)C(F)(F)F
assay
99%
form
liquid
Quality Level
bp
83 °C/12 mmHg (lit.)
density
1.283 g/mL at 25 °C (lit.)
storage temp.
2-8°C
Application
4-（三氟甲基）苯胺用于合成 4-（三烷基甲基）苯胺 。它也被用作合成的构件 。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
A Sgroi et al.
Biochemical and biophysical research communications, 221(2), 361-367 (1996-04-16)
A gene for the Paracentrotus lividus ribosomal protein S24, called P1-S24, has been isolated and sequenced. Ribosomal protein P1-S24 consists 130 amino acids and has a molecular weight of 14869 Da. Sequence analysis shows a high percentage (90%) identity with
L M Angerer et al.
Developmental biology, 149(1), 27-40 (1992-01-01)
We have identified an mRNA that encodes a protein, SpS24, of the small ribosomal subunit in the sea urchin, Strongylocentrotus purpuratus. RNA blot and in situ hybridization analyses show that the SpS24 gene is active during early oogenesis, downregulated in
T Koivula et al.
Gene, 119(1), 145-146 (1992-09-21)
A cloned fragment from Lactococcus lactis chromosome encoding the L33 ribosomal protein was sequenced. Two incomplete open reading frames (ORFs) were also found: the upstream ORF shows similarity to the tetracycline-resistance protein (Tet) of Bacillus stearothermophilus, and the downstream ORF
Tetrahedron Letters, 48, 4749-4749 (2007)
Meritxell Guinó et al.
The Journal of organic chemistry, 72(16), 6290-6293 (2007-07-13)
Optically active torcetrapib was synthesized in seven steps from achiral precursors without the need for protecting groups, utilizing an enantioselective aza-Michael reaction to achieve asymmetry.
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