Methyl 3-nitrothiophene-2-carboxylate

Base Information

Chemical Name:Methyl 3-nitrothiophene-2-carboxylate
CAS No.:75735-44-3
Molecular Formula:C6H5NO4S
Molecular Weight:187.176
Hs Code.:2934999090
DSSTox Substance ID:DTXSID10456559
Nikkaji Number:J693.417J
Wikidata:Q82279110
Mol file:75735-44-3.mol

Synonyms:Methyl 3-nitrothiophene-2-carboxylate;75735-44-3;3-Nitrothiophene-2-carboxylic acid methyl ester;2-Thiophenecarboxylic acid, 3-nitro-, methyl ester;SCHEMBL1848834;DTXSID10456559;DDLFZCCIZTVFBQ-UHFFFAOYSA-N;Methyl3-nitrothiophene-2-carboxylate;CS-0455544;FT-0762405;E87802

Suppliers and Price of Methyl 3-nitrothiophene-2-carboxylate

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

Crysdot
Methyl3-nitrothiophene-2-carboxylate 95+%
1g
$ 510.00

Chemenu
methyl3-nitrothiophene-2-carboxylate 95%
1g
$ 482.00

Arctom
Methyl3-nitrothiophene-2-carboxylate ≥98%
1g
$ 404.00

American Custom Chemicals Corporation
METHYL-3-NITROTHIOPHENE-2-CARBOXYLATE 95.00%
5MG
$ 502.52

Alichem
Methyl3-nitrothiophene-2-carboxylate
1g
$ 453.44

AHH
3-NITROTHIOPHENE-2-CARBOXYLICACIDMETHYLESTER 97%
1g
$ 950.00

Total 5 raw suppliers

Chemical Property of Methyl 3-nitrothiophene-2-carboxylate

Chemical Property:

PSA：100.36000
LogP:1.96610
Storage Temp.:2-8°C
XLogP3:1.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:186.99392881
Heavy Atom Count:12
Complexity:202

Purity/Quality:

97% ^*data from raw suppliers

Methyl3-nitrothiophene-2-carboxylate 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC(=O)C1=C(C=CS1)[N+](=O)[O-]

Technology Process of Methyl 3-nitrothiophene-2-carboxylate

There total 2 articles about Methyl 3-nitrothiophene-2-carboxylate 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: 62.0%

: 5380-42-7
thiophene-2-carboxylic acid methyl ester

: 75735-44-3
Methyl 3-nitrothiophene-2-carboxylate

: 5832-01-9
methyl 5-nitrothiophene-2-carboxylate

Guidance literature:: With trifluoromethylsulfonic anhydride; tetramethylammonium nitrate; In dichloromethane; at 20 ℃; for 42h; Title compound not separated from byproducts.;
DOI:10.1021/jo026202q