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Merck
CN

337633

Sigma-Aldrich

4-氯-2,8-双(三氟甲基)喹啉

97%

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About This Item

经验公式(希尔记法):
C11H4ClF6N
CAS号:
分子量:
299.60
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:

方案

97%

mp

46-48 °C (lit.)

官能团

chloro
fluoro

SMILES字符串

FC(F)(F)c1cc(Cl)c2cccc(c2n1)C(F)(F)F

InChI

1S/C11H4ClF6N/c12-7-4-8(11(16,17)18)19-9-5(7)2-1-3-6(9)10(13,14)15/h1-4H

InChI key

ZSQOESPYYNJBCZ-UHFFFAOYSA-N

一般描述

4-Chloro-2,8-bis(trifluoromethyl)quinolone is the intermediate formed during the synthesis of quinoline derivatives.

象形图

Exclamation mark

警示用语:

Warning

危险声明

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)

235.4 °F - closed cup

闪点(°C)

113 °C - closed cup

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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分析证书(COA)

Lot/Batch Number

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Sumesh Eswaran et al.
European journal of medicinal chemistry, 45(8), 3374-3383 (2010-06-12)
Four new series of quinoline derivatives were synthesized starting from 2-trifluoromethyl aniline through multi-step reactions. In the reaction sequence, substituted aniline was cyclized to 4-hydroxy quinoline 1, which was then transformed to 4-chloro-2,8-bis(trifluoromethyl)quinoline 2. The key scaffold 4-hydrazinyl-2,8-bis(trifluoromethyl)quinoline 3, obtained

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