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412295

4-(三氟甲基)苯肼

Name: 4-(三氟甲基)苯肼
Brand: ALDRICH

96%

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别名:

1-(4-Trifluoromethylphenyl)hydrazine, 4-Trifluoromethylphenylhydrazine, [4-(Trifluoromethyl)phenyl]hydrazine, p-Trifluoromethylphenylhydrazine

线性分子式:

CF₃C₆H₄NHNH₂

CAS号:

368-90-1

分子量:

176.14

MDL编号:

MFCD00042508

PubChem化学物质编号:

24865801

检测方案

96%

bp

118-122 °C/17 mmHg (lit.)

mp

63-65 °C (lit.)

储存温度

2-8°C

SMILES string

NNc1ccc(cc1)C(F)(F)F

InChI

1S/C7H7F3N2/c8-7(9,10)5-1-3-6(12-11)4-2-5/h1-4,12H,11H2

InChI key

DBNLGTYGKCMLLR-UHFFFAOYSA-N

一般描述

4-(Trifluoromethyl)phenylhydrazine participates as phenylhydrazine-based reductant containing fluorine atoms in the one-step reduction and functionalization of graphene oxide.

应用

4-(Trifluoromethyl)phenylhydrazine may be used for the synthesis of 2-iodo-9-trifluoromethyl-paullone.

象形图

GHS07

警示用语：

Warning

危险声明

H315 - H319 - H335

预防措施声明

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

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示例

T1503

货号

25G

包装规格/数量

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705578-5MG-PW

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1000309185

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Fluorine-functionalized and simultaneously reduced graphene oxide as a novel hole transporting layer for highly efficient and stable organic photovoltaic cells.

Su-Hyeon Kim et al.

Nanoscale, 6(13), 7183-7187 (2014-05-08)

A one-step reduction and functionalization of graphene oxide (FrGO) was easily achieved using a novel phenylhydrazine-based reductant containing fluorine atoms, which can induce p-type doping due to its high electronegativity. The FrGO-based OPV exhibited a high power conversion efficiency of

2-Substituted paullones: CDK1/cyclin B-inhibiting property and in vitro antiproliferative activity.

C Kunick et al.

Bioorganic & medicinal chemistry letters, 10(6), 567-569 (2000-03-31)

9-Trifluoromethyl-paullones with a carbon chain in the 2-position were synthesized by palladium-catalyzed coupling reactions of a 2-iodoprecursor with terminal alkenes or alkynes, respectively. The introduction of a 2-cyanoethyl substituent led to a significant enhancement of CDK1/cyclin B inhibiting property and

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