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Merck

412295

Sigma-Aldrich

4-(三氟甲基)苯肼

96%

别名:

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

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About This Item

线性分子式:
CF3C6H4NHNH2
CAS号:
分子量:
176.14
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

96%

bp

118-122 °C/17 mmHg (lit.)

mp

63-65 °C (lit.)

儲存溫度

2-8°C

SMILES 字串

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 密鑰

DBNLGTYGKCMLLR-UHFFFAOYSA-N

一般說明

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

應用

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

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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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
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

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