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T7641

Sigma-Aldrich

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:
Pricing and availability is not currently available.

Quality Level

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.

Warning

Do not heat over 90°C (danger of explosion)

Pictograms

Exploding Bomb

Signal Word

Danger

Hazard 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

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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
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
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
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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