Benzenecarboximidoyl chloride, N-(4-bromophenyl)-

Base Information

Chemical Name:Benzenecarboximidoyl chloride, N-(4-bromophenyl)-
CAS No.:51300-42-6
Molecular Formula:C13H9BrClN
Molecular Weight:294.578
Hs Code.:
DSSTox Substance ID:DTXSID90455181
Mol file:51300-42-6.mol

Synonyms:Benzenecarboximidoyl chloride, N-(4-bromophenyl)-;51300-42-6;DTXSID90455181

Suppliers and Price of Benzenecarboximidoyl chloride, N-(4-bromophenyl)-

Supply Marketing:

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

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Chemical Property of Benzenecarboximidoyl chloride, N-(4-bromophenyl)-

Chemical Property:

XLogP3:5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:292.96069
Heavy Atom Count:16
Complexity:240

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=NC2=CC=C(C=C2)Br)Cl

Technology Process of Benzenecarboximidoyl chloride, N-(4-bromophenyl)-

There total 4 articles about Benzenecarboximidoyl chloride, N-(4-bromophenyl)- 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%

: 7702-38-7
N-(4-bromophenyl)benzamide

: 51300-42-6
N-(4-bromophenyl)benzimidoyl chloride

Guidance literature:: With thionyl chloride; for 4h; Heating;

Reference yield:

: 98-88-4
benzoyl chloride

: 51300-42-6
N-(4-bromophenyl)benzimidoyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 20 °C

2: thionyl chloride / 16 h / Reflux

With thionyl chloride; triethylamine; In dichloromethane;
DOI:10.1039/c9ob02258a

Reference yield:

: 106-40-1
4-bromo-aniline

: 51300-42-6
N-(4-bromophenyl)benzimidoyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 20 °C

2: thionyl chloride / 16 h / Reflux

With thionyl chloride; triethylamine; In dichloromethane;
DOI:10.1039/c9ob02258a