CyclohexylMethyl N-hydroxycarbaMate

Base Information

Chemical Name:CyclohexylMethyl N-hydroxycarbaMate
CAS No.:869111-30-8
Molecular Formula:C8H15NO3
Molecular Weight:173.212
Hs Code.:

Synonyms:CyclohexylMethyl N-hydroxycarbaMate

Suppliers and Price of CyclohexylMethyl N-hydroxycarbaMate

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 3 raw suppliers

Chemical Property of CyclohexylMethyl N-hydroxycarbaMate

Chemical Property:

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of CyclohexylMethyl N-hydroxycarbaMate

There total 3 articles about CyclohexylMethyl N-hydroxycarbaMate 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: 80.0%

: 530-62-1
1,1'-carbonyldiimidazole

: 100-49-2
cyclohexylmethyl alcohol

: 869111-30-8
cyclohexylmethyl N-hydroxycarbamate

Guidance literature:: 1,1'-carbonyldiimidazole; cyclohexylmethyl alcohol; In tetrahydrofuran; at 20 ℃; for 2h;

With hydroxylamine hydrochloride; In pyridine; at 20 ℃; for 6h;
DOI:10.1021/ja0552850

Reference yield:

: C₁₁H₁₆N₂O₂

: 869111-30-8
cyclohexylmethyl N-hydroxycarbamate

Guidance literature:: With 1H-imidazole; hydroxylamine hydrochloride; In acetonitrile; at 20 ℃; for 3.5h; Inert atmosphere;
DOI:10.15227/orgsyn.086.0059

Reference yield:

: 100-49-2
cyclohexylmethyl alcohol

: 869111-30-8
cyclohexylmethyl N-hydroxycarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: acetonitrile / 1.5 h / 0 °C / Inert atmosphere

2: 1H-imidazole; hydroxylamine hydrochloride / acetonitrile / 3.5 h / 20 °C / Inert atmosphere

With 1H-imidazole; hydroxylamine hydrochloride; In acetonitrile;
DOI:10.15227/orgsyn.086.0059