5-tert-butyl-3-methylsulfanyl-1H-1,2,4-triazole

Base Information

Chemical Name:5-tert-butyl-3-methylsulfanyl-1H-1,2,4-triazole
CAS No.:58876-19-0
Molecular Formula:C₇H₁₃N₃S
Molecular Weight:171.266
Hs Code.:
DSSTox Substance ID:DTXSID70372468
Wikidata:Q82160192
ChEMBL ID:CHEMBL1935515

Synonyms:58876-19-0;5-tert-butyl-3-methylsulfanyl-1H-1,2,4-triazole;SCHEMBL6964008;SCHEMBL9344428;CHEMBL1935515;DTXSID70372468;OONCLQJWVPFMKP-UHFFFAOYSA-N;CCG-49943;3-tert.butyl-5-methylthio-1,2,4-4H-triazole;3-tert.butyl-5-methylthio-4H-1,2,4-triazole;SR-01000639361-1;3-tert-butyl-5-(methylsulfanyl)-4H-1,2,4-triazole;Z335958168

Suppliers and Price of 5-tert-butyl-3-methylsulfanyl-1H-1,2,4-triazole

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 5-tert-butyl-3-methylsulfanyl-1H-1,2,4-triazole

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:171.08301860
Heavy Atom Count:11
Complexity:132

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)C1=NC(=NN1)SC

Technology Process of 5-tert-butyl-3-methylsulfanyl-1H-1,2,4-triazole

There total 1 articles about 5-tert-butyl-3-methylsulfanyl-1H-1,2,4-triazole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 62.0%

: 69249-25-8
5-t-Butyl-3-(methylthio)-1,2,4-triazine

: 58876-19-0
3-(tert-butyl)-5-(methylthio)-4H-1,2,4-triazole

: 937-02-0
3-Amino-5-t-butyl-1,2,4-triazine

Guidance literature:: With potassium; ferric nitrate; In ammonia; at -33 ℃; for 5h; Product distribution; Mechanism; Amination of 15N labelled triazine;