T7641
Tetrazole
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About This Item
Empirical Formula (Hill Notation):
CH2N4
CAS Number:
Molecular Weight:
70.05
Beilstein:
105799
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
mp
154-158 °C (lit.)
SMILES string
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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Application
Not recommended for use in DNA synthesis.
Disclaimer
Do not heat over 90°C (danger of explosion)
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Self-react. A
Storage Class Code
1 - Explosive hazardous materials
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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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
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
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