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Benzoic acid, 2-(1-cyclohexen-1-ylmethyl)-2-(trichloroacetyl)hydrazide

Base Information Edit
  • Chemical Name:Benzoic acid, 2-(1-cyclohexen-1-ylmethyl)-2-(trichloroacetyl)hydrazide
  • CAS No.:651311-40-9
  • Molecular Formula:C16H17Cl3N2O2
  • Molecular Weight:375.682
  • Hs Code.:
  • Mol file:651311-40-9.mol
Benzoic acid, 2-(1-cyclohexen-1-ylmethyl)-2-(trichloroacetyl)hydrazide

Synonyms:

Suppliers and Price of Benzoic acid, 2-(1-cyclohexen-1-ylmethyl)-2-(trichloroacetyl)hydrazide
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Benzoic acid, 2-(1-cyclohexen-1-ylmethyl)-2-(trichloroacetyl)hydrazide Edit
Chemical Property:
Purity/Quality:
Safty Information:
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MSDS Files:

SDS file from LookChem

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Technology Process of Benzoic acid, 2-(1-cyclohexen-1-ylmethyl)-2-(trichloroacetyl)hydrazide

There total 2 articles about Benzoic acid, 2-(1-cyclohexen-1-ylmethyl)-2-(trichloroacetyl)hydrazide 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:
Guidance literature:
Multi-step reaction with 2 steps
1.1: CH2Cl2 / 20 °C
2.1: DMAB; methanesulfonic acid / diethyl ether / 3 h / 0 °C
2.2: 81 percent / pyridine / CH2Cl2 / 0 °C
With methanesulfonic acid; In diethyl ether; dichloromethane;
DOI:10.1016/j.tet.2003.10.046
Guidance literature:
Multi-step reaction with 2 steps
1.1: CH2Cl2 / 20 °C
2.1: DMAB; methanesulfonic acid / diethyl ether / 3 h / 0 °C
2.2: 81 percent / pyridine / CH2Cl2 / 0 °C
With methanesulfonic acid; In diethyl ether; dichloromethane;
DOI:10.1016/j.tet.2003.10.046
Guidance literature:
With N,N,N,N,-tetramethylethylenediamine; copper(l) chloride; In acetonitrile; at 60 ℃; for 20h;
DOI:10.1016/j.tet.2003.10.046
upstream raw materials:

1-cyclohexene-1-carboxaldehyde

benzoic acid hydrazide

Downstream raw materials:

gabapentin-lactam

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