Benzamide, N-(1,2,2-trichloroethyl)-

Base Information

Chemical Name:Benzamide, N-(1,2,2-trichloroethyl)-
CAS No.:58956-84-6
Molecular Formula:C9H8Cl3NO
Molecular Weight:252.528
Hs Code.:
DSSTox Substance ID:DTXSID90483141

Synonyms:N-(1,2,2-trichloroethyl)benzamide;Benzamide, N-(1,2,2-trichloroethyl)-;58956-84-6;DTXSID90483141

Suppliers and Price of Benzamide, N-(1,2,2-trichloroethyl)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of Benzamide, N-(1,2,2-trichloroethyl)-

Chemical Property:

XLogP3:3.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:250.967147
Heavy Atom Count:14
Complexity:193

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)NC(C(Cl)Cl)Cl

Technology Process of Benzamide, N-(1,2,2-trichloroethyl)-

There total 5 articles about Benzamide, N-(1,2,2-trichloroethyl)- 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:

: 29431-43-4
N-2,2-dichlorovinylbenzamide

: 58956-84-6
benzoic acid N-1,2,2-trichloromethylamide

Guidance literature:: With hydrogenchloride; diethyl ether;

Reference yield:

: 55-21-0,27208-38-4
benzamide

: 58956-84-6
benzoic acid N-1,2,2-trichloromethylamide

Guidance literature:: Multi-step reaction with 2 steps

1: benzene / Heating

2: SOCl₂

With thionyl chloride; In benzene;

Reference yield:

: 90283-55-9
N-(1-amino-2,2-dichloroethyl)benzamide

: 58956-84-6
benzoic acid N-1,2,2-trichloromethylamide

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / NaNO₂, conc. HCl / H₂O / 24 h / 20 - 25 °C

2: SOCl₂

With hydrogenchloride; thionyl chloride; sodium nitrite; In water;