phenyl 1H-benzo[d][1,2,3]triazol-1-carbiMidothioate

Base Information

Chemical Name:phenyl 1H-benzo[d][1,2,3]triazol-1-carbiMidothioate
CAS No.:141240-69-9
Molecular Formula:C13H10N4S
Molecular Weight:254.3103
Hs Code.:
Mol file:141240-69-9.mol

Synonyms:phenyl 1H-benzo[d][1,2,3]triazol-1-carbiMidothioate

Suppliers and Price of phenyl 1H-benzo[d][1,2,3]triazol-1-carbiMidothioate

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
PHENYL 1H-BENZO[D][1,2,3]TRIAZOLE-1-CARBIMIDOTHIOATE 95.00%
5MG
$ 503.11

Total 2 raw suppliers

Chemical Property of phenyl 1H-benzo[d][1,2,3]triazol-1-carbiMidothioate

Chemical Property:

PSA：79.86000
LogP:3.10620

Purity/Quality:

99% ^*data from raw suppliers

PHENYL 1H-BENZO[D][1,2,3]TRIAZOLE-1-CARBIMIDOTHIOATE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of phenyl 1H-benzo[d][1,2,3]triazol-1-carbiMidothioate

There total 2 articles about phenyl 1H-benzo[d][1,2,3]triazol-1-carbiMidothioate 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: 64.0%

: 108-98-5
thiophenol

: 15328-32-2
1-cyanobenzotriazole

: 141240-69-9
1-(Benzotriazol-1-yl)-1-phenylthiomethanimine

Guidance literature:: In tetrahydrofuran; at 20 ℃; for 1h;

Reference yield:

: 15217-42-2
sodium benzotriazolate

: 141240-69-9
1-(Benzotriazol-1-yl)-1-phenylthiomethanimine

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / tetrahydrofuran / 1 h / 20 °C

2: 64 percent / tetrahydrofuran / 1 h / 20 °C

In tetrahydrofuran; 1: Substitution / 2: Addition;