
CAS 3641-10-9: 1H-1,2,4-Triazole-5-carbonitrile
Formula:C3H2N4
InChI:InChI=1S/C3H2N4/c4-1-3-5-2-6-7-3/h2H,(H,5,6,7)
InChI key:InChIKey=GUQHFZFTGHNVDG-UHFFFAOYSA-N
SMILES:C(#N)C=1NC=NN1
Synonyms:- 1,2,4-Triazole-3-carbonitrile
- 1H-1,2,4-Triazole-3-carbonitrile
- 1H-1,2,4-triazole-5-carbonitrile
- s-Triazole-3-carbonitrile
- 3-Cyano-1,2,4-triazole
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Found 5 products.
1H-1,2,4-Triazole-3-carbonitrile
CAS:1H-1,2,4-Triazole-3-carbonitrileFormula:C3H2N4Purity:By hplc: 99.06% (Typical Value in Batch COA)Color and Shape: white to off-white solidMolecular weight:94.07g/mol3-Cyano-1,2,4-triazole
CAS:3-Cyano-1,2,4-triazole is a nucleophilic compound that is used as a building block for the synthesis of anti-viral agents. It reacts with choline to form an intermediate that can be converted into an active drug by hydrogen bonding to a nucleophile such as chloride or amines. 3-Cyano-1,2,4-triazole has been used in the synthesis of HIV drugs and other compounds that are designed to inhibit viral replication. The process of absorption starts at the mouth and continues through the digestive system into the bloodstream. 3-Cyano-1,2,4-triazole is absorbed from this process and transported to different parts of the body where it can act on its target cells.Formula:C3H2N4Purity:Min. 95%Color and Shape:PowderMolecular weight:94.07 g/mol3-Cyano-1,2,4-triazole
CAS:Controlled ProductApplications A cyano substituted triazole with inhibitory effects on cathepsin K used in a study of the electrophilicity and reactivity of diverse nitrile-containing compounds and its correlation to the mechanism-of-action. References Oballa, R.M. et al.: Bioorg. Med. Chem., 17, 998 (2007);Formula:C3H2N4Color and Shape:NeatMolecular weight:94.072H-1,2,4-triazole-3-carbonitrile
CAS:Purity:95.0%Color and Shape:Solid, Yellow powderMolecular weight:94.07700347900392H-1,2,4-triazole-3-carbonitrile
CAS:Formula:C3H2N4Purity:97%Color and Shape:SolidMolecular weight:94.07477999999999