Methyl 3-[(4-methylbenzoyl)amino]-2-thiophenecarboxylate

Base Information

Chemical Name:Methyl 3-[(4-methylbenzoyl)amino]-2-thiophenecarboxylate
CAS No.:478080-01-2
Molecular Formula:C₁₄H₁₃NO₃S
Molecular Weight:275.328
Hs Code.:
DSSTox Substance ID:DTXSID401202508
ChEMBL ID:CHEMBL1560568

Synonyms:478080-01-2;methyl 3-[(4-methylbenzoyl)amino]-2-thiophenecarboxylate;methyl 3-(4-methylbenzamido)thiophene-2-carboxylate;methyl 3-[(4-methylbenzoyl)amino]thiophene-2-carboxylate;Bionet2_001075;Oprea1_830720;MLS001166157;CHEMBL1560568;DTXSID401202508;HMS1367A19;HMS2855C10;MFCD01348946;AKOS001358718;SMR000550167;CS-0288991;7R-1330;methyl3-(4-methylbenzamido)thiophene-2-carboxylate;Z109088756

Suppliers and Price of Methyl 3-[(4-methylbenzoyl)amino]-2-thiophenecarboxylate

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 2 raw suppliers

Chemical Property of Methyl 3-[(4-methylbenzoyl)amino]-2-thiophenecarboxylate

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:275.06161445
Heavy Atom Count:19
Complexity:340

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=C(C=C1)C(=O)NC2=C(SC=C2)C(=O)OC

Technology Process of Methyl 3-[(4-methylbenzoyl)amino]-2-thiophenecarboxylate

There total 1 articles about Methyl 3-[(4-methylbenzoyl)amino]-2-thiophenecarboxylate 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: 60.0%