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Merck
CN

T7641

四氮唑

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经验公式(希尔记法):
CH2N4
化学文摘社编号:
分子量:
70.05
EC Number:
206-023-4
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
105799
MDL number:
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InChI key

KJUGUADJHNHALS-UHFFFAOYSA-N

InChI

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

SMILES string

c1nnn[nH]1

Quality Level

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Application

Not recommended for use in DNA synthesis.

Disclaimer

切勿加热超过 90°C(爆炸危险)

pictograms

Exploding Bomb

signalword

Danger

hcodes

Hazard Classifications

Self-react. A

存储类别

1 - Explosive hazardous materials

wgk

WGK 3

ppe

Eyeshields, Faceshields, Gloves

法规信息

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分析证书(COA)

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Yann Garcia et al.
Chimia, 67(6), 411-418 (2013-08-16)
The past decade has witnessed intense research activity in the area of Fe(II) spin crossover coordination polymers, which are structurally diverse and functionally intriguing materials. In this endeavor, a less exploited series of ligands have been selected among various N-donor
Xiao-Yang He et al.
Bioorganic & medicinal chemistry, 19(22), 6726-6734 (2011-10-22)
Based on the structure of HIV-1 gp41 binding site for small-molecule inhibitors, optimization of lead 2 resulted in the discovery of a new series of 2,5-dimethyl-3-(5-(N-phenylrhodaninyl)methylene)-N-(3-(1H-tetrazol-5-yl)phenyl)pyrrole compounds with improved anti-HIV-1 activity. The most active compounds 13a and 13j exhibited significant
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
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

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