2-Methyl-1-(4-methylphenyl)sulfonylbenzimidazole

Base Information

Chemical Name:2-Methyl-1-(4-methylphenyl)sulfonylbenzimidazole
CAS No.:15728-46-8
Molecular Formula:C15H14N2O2S
Molecular Weight:286.354
Hs Code.:
DSSTox Substance ID:DTXSID701322389
Nikkaji Number:J3.367.243H
Pharos Ligand ID:SRN5V8WDYHCC
ChEMBL ID:CHEMBL1411903

Synonyms:2-methyl-1-(4-methylphenyl)sulfonylbenzimidazole;15728-46-8;MLS-0350366.0001;2-methyl-1-[(4-methylphenyl)sulfonyl]-1H-benzimidazole;2-methyl-1-(4-methylbenzenesulfonyl)-1H-1,3-benzodiazole;CBMicro_014139;Oprea1_259406;Oprea1_651343;MLS001212204;2-Methyl-1-(toluene-4-sulfonyl)-1H-benzoimidazole;2-methyl-1-tosyl-benzimidazole;cid_755364;CHEMBL1411903;BDBM62312;DTXSID701322389;HMS2835D21;SMSF0004637;STK354003;AKOS000595963;CB09493;SMR000514468;BIM-0014115.P001;US9328112, A10;2-methyl-1-(4-methylphenyl)sulfonyl-benzimidazole;AE-641/02608016;EN300-18236367;SR-01000528219;SR-01000528219-1;Z57112248

Suppliers and Price of 2-Methyl-1-(4-methylphenyl)sulfonylbenzimidazole

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
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price

Total 1 raw suppliers

Chemical Property of 2-Methyl-1-(4-methylphenyl)sulfonylbenzimidazole

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:286.07759887
Heavy Atom Count:20
Complexity:437

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)N2C(=NC3=CC=CC=C32)C

Technology Process of 2-Methyl-1-(4-methylphenyl)sulfonylbenzimidazole

There total 13 articles about 2-Methyl-1-(4-methylphenyl)sulfonylbenzimidazole 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: 87.0%

: 615-15-6
2-Methyl-1H-benzimidazole

: 98-59-9
p-toluenesulfonyl chloride

: 15728-46-8
2-methyl-1-(toluene-4-sulfonyl)-1H-benzimidazole

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃; for 20h; Schlenk technique;
DOI:10.1021/acs.orglett.6b03407

Reference yield: 82.0%

: 615-15-6
2-Methyl-1H-benzimidazole

: 824-79-3
sodium 4-methylbenzenesulfinate

: 15728-46-8
2-methyl-1-(toluene-4-sulfonyl)-1H-benzimidazole

Guidance literature:: With N-Bromosuccinimide; In 1,4-dioxane; at 25 ℃; for 12h;

Reference yield: 73.0%

: C₁₅H₁₆N₂O₂S

: 15728-46-8
2-methyl-1-(toluene-4-sulfonyl)-1H-benzimidazole

Guidance literature:: With [bis(acetoxy)iodo]benzene; potassium carbonate; palladium dichloride; In toluene; at 25 ℃; for 16h; Inert atmosphere;
DOI:10.1002/adsc.201100370