5-benzyl-N-phenyl-1,3,4-thiadiazol-2-amine

Base Information

Chemical Name:5-benzyl-N-phenyl-1,3,4-thiadiazol-2-amine
CAS No.:38376-37-3
Molecular Formula:C15H13N3S
Molecular Weight:267.354
Hs Code.:
DSSTox Substance ID:DTXSID20351142
Nikkaji Number:J2.806.668F
Wikidata:Q82127317
Mol file:38376-37-3.mol

Synonyms:5-benzyl-N-phenyl-1,3,4-thiadiazol-2-amine;38376-37-3;Oprea1_743838;DTXSID20351142;STK756120;AKOS001722934;N-Phenyl-5-benzyl-1,3,4-thiadiazole-2-amine;SR-01000516613;SR-01000516613-1;Z2735124086

Suppliers and Price of 5-benzyl-N-phenyl-1,3,4-thiadiazol-2-amine

Supply Marketing:

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

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Chemical Property of 5-benzyl-N-phenyl-1,3,4-thiadiazol-2-amine

Chemical Property:

XLogP3:4.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:267.08301860
Heavy Atom Count:19
Complexity:262

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CC2=NN=C(S2)NC3=CC=CC=C3

Technology Process of 5-benzyl-N-phenyl-1,3,4-thiadiazol-2-amine

There total 5 articles about 5-benzyl-N-phenyl-1,3,4-thiadiazol-2-amine 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: 96.0%

: 1119010-84-2
2-cyanoethyl phenylcarbamodithioate

: 937-39-3
2-phenylacetylhydrazine

: 38376-37-3
5-benzyl-N-phenyl-1,3,4-thiadiazol-2-amine

Guidance literature:: With water; triethylamine; for 18h; Reflux;
DOI:10.1016/j.tetlet.2009.11.100

Reference yield: 85.0%

: 18233-63-1
N⁴-phenyl-phenylacetic acid thio-semicarbazide

: 38376-37-3
5-benzyl-N-phenyl-1,3,4-thiadiazol-2-amine

Guidance literature:: With manganese (II) nitrate tetrahydrate; at 45 ℃; for 4h;
DOI:10.1016/j.molstruc.2013.09.051

Reference yield:

: 101-41-7
benzeneacetic acid methyl ester

: 38376-37-3
5-benzyl-N-phenyl-1,3,4-thiadiazol-2-amine

Guidance literature:: Multi-step reaction with 3 steps

1: hydrazine hydrate / ethanol / Reflux

2: ethanol / 6 h / 70 °C

3: manganese (II) nitrate tetrahydrate / 4 h / 45 °C

With manganese (II) nitrate tetrahydrate; hydrazine hydrate; In ethanol;
DOI:10.1016/j.molstruc.2013.09.051