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Merck
CN

499412

Sigma-Aldrich

2-噻吩基溴化锌 溶液

0.5 M in THF

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经验公式(希尔记法):
C4H3BrSZn
CAS号:
分子量:
228.43
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.22

质量水平

浓度

0.5 M in THF

密度

0.973 g/mL at 25 °C

储存温度

2-8°C

SMILES字符串

Br[Zn]c1cccs1

InChI

1S/C4H3S.BrH.Zn/c1-2-4-5-3-1;;/h1-3H;1H;/q;;+1/p-1

InChI key

KBBMRTYVFOYNIW-UHFFFAOYSA-M

应用

2-Thienylzinc bromide can be used as:
  • A starting material in the synthesis of heteroaryl sulfonamides by reacting with 2,4,6-trichlorophenyl chlorosulfate.
  • A substrate in the synthesis of naphthacenodithiophene derived polymers, which are used in transistor and solar cell devices.
  • An intermediate in the preparation of isoquinoline derived AICARFT inhibitors.

法律信息

Rieke® Metals, Inc. 的产品,®Rieke Metals, Inc. 的注册商标

警示用语:

Danger

危险分类

Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3

靶器官

Respiratory system

补充剂危害

WGK

WGK 3

闪点(°F)

-0.0 °F

闪点(°C)

-17.78 °C

法规信息

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Discovery of N-(6-Fluoro-1-oxo-1, 2-dihydroisoquinolin-7-yl)-5-[(3 R)-3-hydroxypyrrolidin-1-yl] thiophene-2-sulfonamide (LSN 3213128), a Potent and Selective Nonclassical Antifolate Aminoimidazole-4-carboxamide Ribonucleotide Formyltransferase (AICARFT) Inhibitor Effective at Tumor Suppression in a Cancer Xenograft Model
Fales KR, et al.
Journal of Medicinal Chemistry, 60(23), 9599-9616 (2017)
Naphthacenodithiophene based polymers-new members of the acenodithiophene family exhibiting high mobility and power conversion efficiency
Knall A-C, et al.
Advances in Functional Materials, 26(38), 6961-6969 (2016)
Synthesis of Heteroaryl Sulfonamides from Organozinc Reagents and 2, 4, 6-Trichlorophenyl Chlorosulfate
Colombe JR, et al.
Organic Letters, 17(12), 3170-3173 (2015)

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