CAS 6818-99-1
:5-Chloro-1H-1,2,4-triazole
Description:
5-Chloro-1H-1,2,4-triazole is a heterocyclic compound characterized by its five-membered ring structure containing three nitrogen atoms and two carbon atoms. The presence of a chlorine atom at the 5-position of the triazole ring contributes to its unique chemical properties. This compound is typically a white to off-white crystalline solid and is soluble in polar solvents such as water and alcohols. It exhibits a range of biological activities, making it of interest in agricultural and pharmaceutical applications, particularly as a fungicide and in the synthesis of various bioactive molecules. The triazole ring is known for its ability to form hydrogen bonds, which can enhance its interactions with biological targets. Additionally, 5-Chloro-1H-1,2,4-triazole can undergo various chemical reactions, including substitution and coupling reactions, which are valuable in organic synthesis. Its stability and reactivity make it a versatile compound in both research and industrial settings.
Formula:C2H2ClN3
InChI:InChI=1S/C2H2ClN3/c3-2-4-1-5-6-2/h1H,(H,4,5,6)
InChI key:InChIKey=QGOUKZPSCTVYLX-UHFFFAOYSA-N
SMILES:ClC=1NC=NN1
Synonyms:- 1H-1,2,4-Triazole, 3-chloro-
- 1H-1,2,4-Triazole, 5-chloro-
- 3-Chloro-1,2,4-triazole
- 3-Chloro-s-triazole
- 3-chloro-4,5-dihydro-1H-1,2,4-triazole
- 5-Chloro-1H-[1,2,4]triazol-3-ylamine
- 5-chloro-1H-1,2,4-triazole
- Nsc 153381
- s-Triazole, 3-chloro-
- s-Triazole, 3-chloro- (VAN) (8CI)
- 3-Chloro-1H-1,2,4-triazole
- See more synonyms
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Found 5 products.
3-Chloro-1,2,4-triazole
CAS:Formula:C2H2ClN3Purity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:103.513-Chloro-1H-1,2,4-triazole
CAS:<p>3-Chloro-1H-1,2,4-triazole</p>Purity:97%Color and Shape:Off-White PowderMolecular weight:103.51g/mol3-Chloro-1,2,4-triazole
CAS:Formula:C2H2ClN3Purity:96%Color and Shape:Yellow powderMolecular weight:103.513-Chloro-1,2,4-triazole
CAS:<p>3-Chloro-1,2,4-triazole is a nucleophilic compound that is used to synthesize amitrole and other heterocyclic compounds. It reacts with 4-methoxyphenylboronic acid in the presence of histidine to form an acyl chloride. 3-Chloro-1,2,4-triazole also reacts with triazole in the presence of a copper catalyst to form an alkylating agent. The nitro group can be converted into a chloro group by treatment with sodium hypochlorite. 3-Chloro-1,2,4-triazole has been shown to inhibit weed growth by inhibiting catalase and other enzymes responsible for nitrogen fixation.</p>Formula:C2H2ClN3Purity:Min. 95%Color and Shape:White To Light (Or Pale) Yellow SolidMolecular weight:103.51 g/mol




