跳转至内容
Merck
CN

102520

4-氨基-2,1,3-苯并噻二唑

98%

别名:

4-氨基苯并-2,1,3-噻二唑

登录 查看组织和合同定价。

选择尺寸


关于此项目

经验公式(希尔记法):
C6H5N3S
化学文摘社编号:
分子量:
151.19
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
212-186-2
MDL number:
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

产品名称

4-氨基-2,1,3-苯并噻二唑, 98%

InChI key

DRLGIZIAMHIQHL-UHFFFAOYSA-N

InChI

1S/C6H5N3S/c7-4-2-1-3-5-6(4)9-10-8-5/h1-3H,7H2

SMILES string

Nc1cccc2nsnc12

assay

98%

form

solid

mp

67-69 °C (lit.)

Application

4-Amino-2,1,3-benzothiadiazole was used in a study to synthesize and evaluate the inhibitory activity of a series of substituted benzimidazoles and small benzothiadiazoles on rat liver methionine synthase. It was used as potential levelers for Cu plating in submicrometer trenches.

General description

4-Amino-2,1,3-benzothiadiazole is a gold green to yellow brown powder. It undergoes palladium catalyzed C-N coupling with 2-(2′-bromo-9′,9′-diethylfluoren-7′-yl)-9,9-diethylfluorene to form novel fluorescent dyes. 4-Amino-2,1,3-benzothiadiazole forms dicopper complexes.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

存储类别

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

法规信息

新产品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

[Comparative evaluation of the effectiveness of radioprotective agents judged from their protection of bone marrow and the gastrointestinal tract].
N N Piatovskaia et al.
Radiobiologiia, 22(2), 183-186 (1982-03-01)
Rapid galvanostatic determination on levelers for superfilling in Cu electroplating.
Electrochemical and Solid-State Letters, 13(2), D7-D10 (2010)
Solution-processable organic fluorescent dyes for multicolor emission in organic light emitting diodes.
Pu YJ, et al.
Journal of Materials Chemistry, 18(35), 4183-4188 (2008)
Elizabeth C Banks et al.
The FEBS journal, 274(1), 287-299 (2007-01-16)
The cobalamin-dependent cytosolic enzyme, methionine synthase (EC.2.1.1.13), catalyzes the remethylation of homocysteine to methionine using 5-methyltetrahydrofolate as the methyl donor. The products of this remethylation--methionine and tetrahydrofolate--participate in the active methionine and folate pathways. Impaired methionine synthase activity has been
Rapid galvanostatic determination on levelers for superfilling in Cu electroplating.
Tsai HC, et al.
Electrochemical and Solid-State Letters, 13(2), D7-D10 (2010)

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持