2(1H)-Quinoxalinone, 3-(2-thienyl)-

Base Information

Chemical Name:2(1H)-Quinoxalinone, 3-(2-thienyl)-
CAS No.:64532-10-1
Molecular Formula:C12H8N2OS
Molecular Weight:
Hs Code.:
DSSTox Substance ID:DTXSID20352351
Nikkaji Number:J3.388.141J
Wikidata:Q82129440
ChEMBL ID:CHEMBL1320709

Synonyms:64532-10-1;2(1H)-Quinoxalinone, 3-(2-thienyl)-;3-(Thiophen-2-yl)quinoxalin-2(1H)-one;3-thiophen-2-yl-1H-quinoxalin-2-one;3-(2-Thienyl)-2(1H)-quinoxalinone;MLS000053745;3-(thiophen-2-yl)-1,2-dihydroquinoxalin-2-one;SMR000068248;3-(2-thienyl)-1,2-dihydroquinoxalin-2-one;HMS1443J08;Maybridge3_004430;SCHEMBL578071;cid_723698;CHEMBL1320709;BDBM39463;DTXSID20352351;PWIKCZVHLJFOFW-UHFFFAOYSA-N;HMS2377C17;3-(Thiophen-2-yl)quinoxalin-2-ol;3(2-thienyl)quinoxalin-2(1H)-one;MFCD00663403;3(2-thienyl)quinoxalin-2(1 H)-one;3-(2-thienyl)-1H-quinoxalin-2-one;3-(2-thienyl)quinoxalin-2(1H)-one;AKOS002534818;2(1h)-quinoxalinone,3-(2-thienyl)-;CCG-251040;3-(2-thienyl)quinoxalin-2(1 H)-one;IDI1_015817;TS-03241;CS-0326737

Suppliers and Price of 2(1H)-Quinoxalinone, 3-(2-thienyl)-

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

Total 5 raw suppliers

Chemical Property of 2(1H)-Quinoxalinone, 3-(2-thienyl)-

Chemical Property:

XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:228.03573406
Heavy Atom Count:16
Complexity:329

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C2C(=C1)NC(=O)C(=N2)C3=CC=CS3

Technology Process of 2(1H)-Quinoxalinone, 3-(2-thienyl)-

There total 6 articles about 2(1H)-Quinoxalinone, 3-(2-thienyl)- 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: 99.0%

: 4075-59-6
2-thiopheneglyoxylic acid

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

: 64532-10-1
3-(thiophen-2-yl)quinoxalin-2(1H)-one

Guidance literature:: With air; In water; at 110 ℃; for 1h; Green chemistry;
DOI:10.1021/acs.joc.1c01497

Reference yield: 72.0%

: 4075-59-6
2-thiopheneglyoxylic acid

: 1029649-48-6
tert-butyl (2-isocyanophenyl)carbamate

: 64532-10-1
3-(thiophen-2-yl)quinoxalin-2(1H)-one

Guidance literature:: 2-thiopheneglyoxylic acid; tert-butyl (2-isocyanophenyl)carbamate; In 1,2-dichloro-ethane; at 150 ℃; for 10h; Microwave irradiation;

With trifluoroacetic acid; In 1,2-dichloro-ethane; at 100 ℃; for 0.166667h; Microwave irradiation;
DOI:10.1055/s-0034-1379016