3-Thiophenecarboxamide, 2-[(aminocarbonyl)amino]-5-bromo-

Base Information

Chemical Name:3-Thiophenecarboxamide, 2-[(aminocarbonyl)amino]-5-bromo-
CAS No.:354812-10-5
Molecular Formula:C6H6BrN3O2S
Molecular Weight:264.103
Hs Code.:

Synonyms:5-Bromo-2-ureidothiophene-3-carboxamide;5-bromo-2-ureido-thiophene-3-carboxylic acid amide;

Suppliers and Price of 3-Thiophenecarboxamide, 2-[(aminocarbonyl)amino]-5-bromo-

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
5-Bromo-2-ureidothiophene-3-carboxamide 95+%
1g
$ 491.00

Chemenu
5-Bromo-2-ureidothiophene-3-carboxamide 95%
1g
$ 464.00

Arctom
5-Bromo-2-ureidothiophene-3-carboxamide ≥95%
1g
$ 401.00

Total 1 raw suppliers

Chemical Property of 3-Thiophenecarboxamide, 2-[(aminocarbonyl)amino]-5-bromo-

Chemical Property:

PSA：128.43000
LogP:2.57110

Purity/Quality:: 5-Bromo-2-ureidothiophene-3-carboxamide 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 3-Thiophenecarboxamide, 2-[(aminocarbonyl)amino]-5-bromo-

There total 3 articles about 3-Thiophenecarboxamide, 2-[(aminocarbonyl)amino]-5-bromo- 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: 89.0%

: 633309-16-7
5-bromo-2-[3-(2,2,2-trichloro-ethanoyl)-ureido]-thiophene-3-carboxylic acid amide

: 354812-10-5
2-[(aminocarbonyl)amino]-5-bromo-3-thiophenecarboxamide

Guidance literature:: With sodium carbonate; In ethanol; water;

Reference yield: 71.0%

: 339365-14-9
1-(3-carbamoylthiophen-2-yl)urea

: 354812-10-5
2-[(aminocarbonyl)amino]-5-bromo-3-thiophenecarboxamide

Guidance literature:: With N-Bromosuccinimide; In tetrahydrofuran; at 0 - 20 ℃; for 16h; Inert atmosphere; Darkness;
DOI:10.3987/COM-19-S(F)43

Reference yield:

: 14080-51-4
2-aminothiophene-3-carboxamide

: 354812-10-5
2-[(aminocarbonyl)amino]-5-bromo-3-thiophenecarboxamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: acetonitrile / 3.5 h / 0 - 20 °C / Inert atmosphere

1.2: 15 h / 0 - 20 °C / Inert atmosphere

2.1: N-Bromosuccinimide / tetrahydrofuran / 16 h / 0 - 20 °C / Inert atmosphere; Darkness

With N-Bromosuccinimide; In tetrahydrofuran; acetonitrile;
DOI:10.3987/COM-19-S(F)43