N-Benzhydryl-2-bromoacetamide

Base Information

Chemical Name:N-Benzhydryl-2-bromoacetamide
CAS No.:119706-03-5
Molecular Formula:C15H14BrNO
Molecular Weight:304.186
Hs Code.:
DSSTox Substance ID:DTXSID30557138
Nikkaji Number:J3.191.499J
Wikidata:Q82438936

Synonyms:N-Benzhydryl-2-bromoacetamide;119706-03-5;SCHEMBL5148694;DTXSID30557138;HCYGPROWCVVTHE-UHFFFAOYSA-N;2-Bromo-N-(diphenylmethyl)acetamide;AKOS012990640;N-Benzhydryl-2-bromoacetamide, AldrichCPR

Suppliers and Price of N-Benzhydryl-2-bromoacetamide

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of N-Benzhydryl-2-bromoacetamide

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:303.02588
Heavy Atom Count:18
Complexity:239

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(C2=CC=CC=C2)NC(=O)CBr

Technology Process of N-Benzhydryl-2-bromoacetamide

There total 3 articles about N-Benzhydryl-2-bromoacetamide 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:

: 22118-09-8
2-bromoacetyl chloride

: 91-00-9
Benzhydrylamine

: 119706-03-5
N-benzhydryl-2-bromoacetamide

Guidance literature:: With triethylamine; In N,N-dimethyl-formamide; for 1h;
DOI:10.1021/ja0302836

Reference yield:

: 598-21-0
2-Bromoacetyl bromide

: 91-00-9
Benzhydrylamine

: 119706-03-5
N-benzhydryl-2-bromoacetamide

Guidance literature:: In triethylamine;

Reference yield:

: 79-08-3
bromoacetic acid

: 91-00-9
Benzhydrylamine

: 119706-03-5
N-benzhydryl-2-bromoacetamide

Guidance literature:: With 1-hydroxy-pyrrolidine-2,5-dione; dicyclohexyl-carbodiimide; Yield given. Multistep reaction; 1.) 1,2-dimethoxyethane, 3 h, 0 degC; 2.) 1 h, room temp.;
DOI:10.1016/S0040-4020(01)86014-2