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224936

4-(三氟甲基)苯胺

Name: 4-(三氟甲基)苯胺
Brand: ALDRICH

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:

455-14-1

分子量:

161.12

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24853465

EC Number:

207-236-5

Beilstein/REAXYS Number:

1564853

MDL number:

MFCD00064396

Assay:

99%

Form:

liquid

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Quality Level

200

assay

99%

form

liquid

refractive index

n20/D 1.483 (lit.)

bp

83 °C/12 mmHg (lit.)

density

1.283 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

Nc1ccc(cc1)C(F)(F)F

InChI

1S/C7H6F3N/c8-7(9,10)5-1-3-6(11)4-2-5/h1-4H,11H2

InChI key

ODGIMMLDVSWADK-UHFFFAOYSA-N

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。

pictograms

GHS06,GHS05,GHS09

signalword

Danger

hcodes

H301,H318,H410

pcodes

P264 - P273 - P280 - P301 + P310 - P305 + P351 + P338 - P391

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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A Facile Synthesis of 4-(Trialkylmethyl) anilines by the Reaction of 4-(Trifluoromethyl) aniline with Grignard Reagents.

Synthetic Communications, 27(11), 1975-1980 (1997)

Tetrahedron Letters, 48, 4749-4749 (2007)

A concise asymmetric synthesis of torcetrapib.

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.

Hamster ribosomal protein S24 multigene family: genomic organization and molecular structure of two pseudogenes.

H Klein

Biochemistry and cell biology = Biochimie et biologie cellulaire, 75(2), 177-182 (1997-01-01)

A cDNA coding for the hamster S24 ribosomal protein was used to isolate homologous genes from a Syrian hamster fibroblast genomic library. Southern analysis, using S24 ribosomal protein cDNA and two probes derived from the 5' and 3' ends, suggests

Trifluoromethylanilines--their effect on DNA synthesis and proliferative activity in parenchymal organs of rats.

J Seifert et al.

Toxicology, 83(1-3), 49-59 (1993-10-25)

Reactive isomeric 3- and 4-trifluoromethylanilines (3-,4-TFMA), and control aniline itself, induced the following effects on biosynthesis of DNA in the liver, kidney, thymus and spleen of rats: (a) The administration of 4-TFMA initially suppressed the utilization of labeled thymidine for

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全球贸易项目编号

货号	GTIN
224936-25G	04061838779335
224936-10G	04061838779311
224936-1G	04061838779328

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