1,3,4-Thiadiazol-2-amine, 5-(2-cyclohexylethenyl)-, (E)-

Base Information

Chemical Name:1,3,4-Thiadiazol-2-amine, 5-(2-cyclohexylethenyl)-, (E)-
CAS No.:118314-09-3
Molecular Formula:C₁₀H₁₅N₃S
Molecular Weight:209.315
Hs Code.:
DSSTox Substance ID:DTXSID401199173

Synonyms:DTXSID401199173;1,3,4-Thiadiazol-2-amine, 5-(2-cyclohexylethenyl)-, (E)-;118314-09-3

Suppliers and Price of 1,3,4-Thiadiazol-2-amine, 5-(2-cyclohexylethenyl)-, (E)-

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 1,3,4-Thiadiazol-2-amine, 5-(2-cyclohexylethenyl)-, (E)-

Chemical Property:

XLogP3:3.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:209.09866866
Heavy Atom Count:14
Complexity:202

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CCC(CC1)C=CC2=NN=C(S2)N
Isomeric SMILES:C1CCC(CC1)/C=C/C2=NN=C(S2)N

Technology Process of 1,3,4-Thiadiazol-2-amine, 5-(2-cyclohexylethenyl)-, (E)-

There total 2 articles about 1,3,4-Thiadiazol-2-amine, 5-(2-cyclohexylethenyl)-, (E)- 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: 34.8%

: 6050-00-6
3-cyclohexane-2-propenenitrile

: 79-19-6
thiosemicarbazide

: 118314-09-3
5-((E)-2-Cyclohexyl-vinyl)-[1,3,4]thiadiazol-2-ylamine

Guidance literature:: With trifluoroacetic acid;
DOI:10.1248/cpb.40.2391

Reference yield:

: 2043-61-0
cyclohexanecarbaldehyde

: 118314-09-3
5-((E)-2-Cyclohexyl-vinyl)-[1,3,4]thiadiazol-2-ylamine

Guidance literature:: Multi-step reaction with 2 steps

1: 94.1 percent / 40percent aq. NaOH / CH₂Cl₂ / 2 h / Ambient temperature

2: 34.8 percent / CF₃COOH

With sodium hydroxide; trifluoroacetic acid; In dichloromethane;
DOI:10.1248/cpb.40.2391