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Merck
CN

247154

Sigma-Aldrich

3,4-二溴噻吩

99%

别名:

3,4-二溴噻吩

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About This Item

经验公式(希尔记法):
C4H2Br2S
CAS号:
分子量:
241.93
Beilstein:
107642
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

99%

形式

liquid

折射率

n20/D 1.640 (lit.)

bp

221-222 °C (lit.)

mp

4-5 °C (lit.)

密度

2.188 g/mL at 25 °C (lit.)

SMILES字符串

Brc1cscc1Br

InChI

1S/C4H2Br2S/c5-3-1-7-2-4(3)6/h1-2H

InChI key

VGKLVWTVCUDISO-UHFFFAOYSA-N

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一般描述

已通过基于电子飞行时间测量的符合光谱技术对3,4-二溴噻吩的双光电离光谱进行了研究

应用

3,4-二溴噻吩已被用于制备噻吩并[3,4-b]噻吩。它也作为起始材料用于合成烷基取代的稠合噻吩

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

WGK

WGK 3

闪点(°F)

closed cup

闪点(°C)

closed cup

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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P Linusson et al.
The Journal of chemical physics, 129(23), 234303-234303 (2008-12-24)
We report the double photoionization spectra of thiophene, 3-bromothiophene, and 3,4-dibromothiophene using a coincidence spectroscopy technique based on electron time-of-flight measurements. Spectra have been recorded between the onset and 40.814 eV using He IIalpha radiation. The He I photoelectron spectrum
An Alternative Synthysis of Thieno [3, 4-b] Thiophene.
Brandsma L and Verkruijsse HD.
Synthetic Communications, 20(15), 2275-2277 (1990)
Mingqian He et al.
The Journal of organic chemistry, 72(2), 442-451 (2007-01-16)
We have established a series of synthetic methods to synthesize alkyl-substituted fused thiophenes with degrees of fusion from two to seven rings. These fused thiophene ring compounds have very good solubility in common organic solvents, making possible the solution processing

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