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Merck
CN

T7641

Sigma-Aldrich

四氮唑

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关于此项目

经验公式(希尔记法):
CH2N4
化学文摘社编号:
分子量:
70.05
Beilstein:
105799
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
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mp

154-158 °C (lit.)

SMILES字符串

c1nnn[nH]1

InChI

1S/CH2N4/c1-2-4-5-3-1/h1H,(H,2,3,4,5)

InChI key

KJUGUADJHNHALS-UHFFFAOYSA-N

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应用

Not recommended for use in DNA synthesis.

免责声明

切勿加热超过 90°C(爆炸危险)

象形图

Exploding Bomb

警示用语:

Danger

危险声明

危险分类

Self-react. A

储存分类代码

1 - Explosive hazardous materials

WGK

WGK 3

个人防护装备

Eyeshields, Faceshields, Gloves

法规信息

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Xiaobao Xu et al.
Nanoscale, 5(17), 7963-7969 (2013-07-19)
Herein, an organic redox couple 1-methy-1H-tetrazole-5-thiolate (T(-)) and its disulfide dimer (T2) redox shuttle, as an electrolyte, is introduced in a p-type dye-sensitized solar cell (DSC) on the basis of an organic dye (P1) sensitizer and nanocrystal CuCrO2 electrode. Using
An approach to the site-selective deoxygenation of hydroxy groups based on catalytic phosphoramidite transfer.
Peter A Jordan et al.
Angewandte Chemie (International ed. in English), 51(12), 2907-2911 (2012-02-10)
Michael Limbach
Chemistry & biodiversity, 3(2), 119-133 (2006-12-29)
Catalytic enantioselective methodology has dramatically been enriched by the re-discovery of the simple amino acid proline as a chiral catalyst in the year 2000. Although no catalyst offers such a simple and broad access to quite complex reaction products, as
Satsuki Otsuki et al.
Bioorganic & medicinal chemistry letters, 23(6), 1608-1611 (2013-02-19)
Irreversible modification is one of the most promising strategies to identify cellular receptors of bioactive small molecules. Here we report that receptor proteins can be chemically tagged using a 5-sulfonyl tetrazole probe. 5-Sulfonyl tetrazole easily accepted nucleophilic attack of thiol
Falgun Shah et al.
Journal of chemical information and modeling, 52(3), 696-710 (2012-02-16)
Falcipains (FPs) are hemoglobinases of Plasmodium falciparum that are validated targets for the development of antimalarial chemotherapy. A combined ligand- and structure-based virtual screening of commercial databases was performed to identify structural analogs of virtual screening hits previously discovered in

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