1H-Benzimidazole-2-carbothioamide

Base Information

Chemical Name:1H-Benzimidazole-2-carbothioamide
CAS No.:35369-17-6
Molecular Formula:C8H7 N3 S
Molecular Weight:177.23
Hs Code.:2933990090
DSSTox Substance ID:DTXSID20418724
Mol file:35369-17-6.mol

Synonyms:1H-Benzimidazole-2-carbothioamide;35369-17-6;1H-BENZO[D]IMIDAZOLE-2-CARBOTHIOAMIDE;1H-Benzimidazole-2-carbothioamide(9CI);Benzimidazole-3-thiocarboxamide;benzimidazole-2-carbothioamide;SCHEMBL6028990;DTXSID20418724;SZWRKUVGGWEDCP-UHFFFAOYSA-N;1H-Benzimidazole-2-carbothioamide #;AKOS015995221;S11233;J-504654

Suppliers and Price of 1H-Benzimidazole-2-carbothioamide

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
1H-BENZIMIDAZOLE-2-CARBOTHIOAMIDE 95.00%
5MG
$ 495.20

AccelPharmtech
1H-Benzimidazole-2-carbothioamide 97.00%
25G
$ 9900.00

AccelPharmtech
1H-Benzimidazole-2-carbothioamide 97.00%
5G
$ 5270.00

AccelPharmtech
1H-Benzimidazole-2-carbothioamide 97.00%
1G
$ 3060.00

Total 1 raw suppliers

Chemical Property of 1H-Benzimidazole-2-carbothioamide

Chemical Property:

PSA：86.79000
LogP:1.89740
XLogP3:1.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:177.03606841
Heavy Atom Count:12
Complexity:195

Purity/Quality:: 1H-BENZIMIDAZOLE-2-CARBOTHIOAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)NC(=N2)C(=S)N

Technology Process of 1H-Benzimidazole-2-carbothioamide

There total 6 articles about 1H-Benzimidazole-2-carbothioamide 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: 61.2%

: 5805-52-7
1H-benzo[d]imidazole-2-carboxamide

: 35369-17-6
1H-benzo[d]imidazole-2-carbothioamide

Guidance literature:: With Lawessons reagent; In tetrahydrofuran; at 66 ℃; for 5h;
DOI:10.3390/molecules24071198

Reference yield:

: 2849-93-6
2-benzimidazolecarboxylic acid

: 35369-17-6
1H-benzo[d]imidazole-2-carbothioamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: thionyl chloride / 4 h / 79 °C

1.2: 5 h / 70 °C

2.1: Lawessons reagent / tetrahydrofuran / 5 h / 66 °C

With Lawessons reagent; thionyl chloride; In tetrahydrofuran;

Reference yield:

: 95-54-5
1,2-diamino-benzene

: 35369-17-6
1H-benzo[d]imidazole-2-carbothioamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogenchloride / water / 4 h / 100 °C

2.1: potassium carbonate; potassium permanganate / water / 1 h / 100 °C / Reflux

3.1: thionyl chloride / 4 h / 79 °C

3.2: 5 h / 70 °C

4.1: Lawessons reagent / tetrahydrofuran / 5 h / 66 °C

With Lawessons reagent; hydrogenchloride; potassium permanganate; thionyl chloride; potassium carbonate; In tetrahydrofuran; water;