N-[[3-(Acetylamino)-4-chlorophenyl]methyl]-2-chloroacetamide

Base Information

Chemical Name:N-[[3-(Acetylamino)-4-chlorophenyl]methyl]-2-chloroacetamide
CAS No.:102677-67-8
Molecular Formula:C₁₁H₁₂Cl₂N₂O₂
Molecular Weight:275.134
Hs Code.:
DSSTox Substance ID:DTXSID201186522

Synonyms:DTXSID201186522;N-[[3-(Acetylamino)-4-chlorophenyl]methyl]-2-chloroacetamide;102677-67-8

Suppliers and Price of N-[[3-(Acetylamino)-4-chlorophenyl]methyl]-2-chloroacetamide

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of N-[[3-(Acetylamino)-4-chlorophenyl]methyl]-2-chloroacetamide

Chemical Property:

XLogP3:1.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:274.0275830
Heavy Atom Count:17
Complexity:287

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(=O)NC1=C(C=CC(=C1)CNC(=O)CCl)Cl

Technology Process of N-[[3-(Acetylamino)-4-chlorophenyl]methyl]-2-chloroacetamide

There total 1 articles about N-[[3-(Acetylamino)-4-chlorophenyl]methyl]-2-chloroacetamide 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:

: 2832-19-1
2-Chloro-N-(hydroxymethyl)acetamide

: 533-17-5
N-(2-chlorophenyl)acetamide

: 102677-67-8
N-(3-Acetylamino-4-chloro-benzyl)-2-chloro-acetamide

Guidance literature:: With sulfuric acid; for 24h; Ambient temperature;

Reference yield:

: 102677-67-8
N-(3-Acetylamino-4-chloro-benzyl)-2-chloro-acetamide

: 104-86-9
4-chlorobenzylamine

Guidance literature:: Multi-step reaction with 2 steps

1: aq. HCl / 2 h / Heating

2: 1.) NaNO₂, aq. HCl, 2.) aq. hypophosphorous acid / 2.) 15 min

With hydrogenchloride; hypophosphorous acid; sodium nitrite;