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Merck

232947

Sigma-Aldrich

2-(三氟甲基)苯甲腈

98%

别名:

α,α,α-三氟邻甲基苯甲腈

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About This Item

线性分子式:
CF3C6H4CN
CAS号:
分子量:
171.12
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:

方案

98%

折射率

n20/D 1.4632 (lit.)

mp

7.5 °C (lit.)

密度

1.294 g/mL at 25 °C (lit.)

SMILES字符串

FC(F)(F)c1ccccc1C#N

InChI

1S/C8H4F3N/c9-8(10,11)7-4-2-1-3-6(7)5-12/h1-4H

InChI key

SOZGHDCEWOLLHV-UHFFFAOYSA-N

一般描述

2-(Trifluoromethyl)benzonitrile reacts with tert-butyl acetate in the presence of sulfuric acid to give the corresponding N-tert-butyl amides.

应用

2-(Trifluoromethyl)benzonitrile was used in the synthesis of symmetrical N,N′-alkylidine bisamides.

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

储存分类代码

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

WGK

WGK 2

闪点(°F)

194.0 °F - closed cup

闪点(°C)

90 °C - closed cup

个人防护装备

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 convenient and efficient protocol for the synthesis of symmetrical N,N'-alkylidine bisamides by sulfamic acid under solvent-free conditions.
Selvam NP, et al.
Canadian Journal of Chemistry, 86(1), 32-38 (2008)
An efficient method for the conversion of aromatic and aliphatic nitriles to the corresponding N-tert-butyl amides: a modified Ritter reaction.
Reddy KL.
Tetrahedron Letters, 44(7), 1453-1455 (2003)
Megumi Morimoto et al.
PloS one, 12(12), e0189480-e0189480 (2017-12-08)
Sarcopenia and cachexia present characteristic features of a decrease in skeletal muscle mass and strength, anorexia, and lack of motivation. Treatments for these diseases have not yet been established, although selective androgen receptor modulators (SARMs) are considered as therapeutic targets.
Nobuyuki Ishikura et al.
International journal of oncology, 46(4), 1560-1572 (2015-01-31)
Resistance of prostate cancer to castration is currently an unavoidable problem. The major mechanisms underlying such resistance are androgen receptor (AR) overexpression, androgen-independent activation of AR, and AR mutation. To address this problem, we developed an AR pure antagonist, CH5137291

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