o-Chlorophenylcyanamide

Base Information

Chemical Name:o-Chlorophenylcyanamide
CAS No.:45765-25-1
Molecular Formula:C7H5ClN2
Molecular Weight:152.583
Hs Code.:2926909090
Mol file:45765-25-1.mol

Synonyms:2-CHLOROPHENYLCYANAMIDE

Suppliers and Price of o-Chlorophenylcyanamide

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

TRC
[(2-chlorophenyl)amino]carbonitrile
10mg
$ 45.00

AK Scientific
O-Chlorophenylcyanamide
2.5g
$ 1459.00

AK Scientific
O-Chlorophenylcyanamide
100mg
$ 294.00

Total 3 raw suppliers

Chemical Property of o-Chlorophenylcyanamide

Chemical Property:

PSA：35.82000
LogP:2.30598

Purity/Quality:

95% ^*data from raw suppliers

[(2-chlorophenyl)amino]carbonitrile ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of o-Chlorophenylcyanamide

There total 13 articles about o-Chlorophenylcyanamide 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: 95.0%

: 56935-60-5
2-chloro-benzamide oxime

: 45765-25-1
(2-chlorophenyl)cyanamide

Guidance literature:: With 2-Nitrobenzenesulfonyl chloride; In pyridine; at 0 - 20 ℃; Solvent; Inert atmosphere;
DOI:10.1021/ol403645y

Reference yield: 95.0%

: 622-34-4
1-phenylcyanamide

: 45765-25-1
(2-chlorophenyl)cyanamide

Guidance literature:: With N-chloro-succinimide; 2,6-di-tert-butyl-4-methyl-phenol; palladium diacetate; In 1,2-dichloro-ethane; at 80 ℃; for 8h; regioselective reaction; Green chemistry;
DOI:10.1039/d1nj01998h