O-benzyl-N-isopropylhydroxylamine

Base Information

Chemical Name:O-benzyl-N-isopropylhydroxylamine
CAS No.:136943-84-5
Molecular Formula:C₁₀H₁₅NO
Molecular Weight:165.235
Hs Code.:

Synonyms:O-benzyl-N-isopropylhydroxylamine

Suppliers and Price of O-benzyl-N-isopropylhydroxylamine

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 0 raw suppliers

Chemical Property of O-benzyl-N-isopropylhydroxylamine

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of O-benzyl-N-isopropylhydroxylamine

There total 3 articles about O-benzyl-N-isopropylhydroxylamine 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: 92.0%

: 3376-36-1
acetone O-benzyloxime

: 136943-84-5
O-benzyl-N-isopropylhydroxylamine

Guidance literature:: With hydrogenchloride; sodium cyanoborohydride; In methanol; at 20 ℃; for 16h; pH=3 - 4;
DOI:10.1016/S0040-4020(00)00721-3

Reference yield:

: 2687-43-6
O-benzylhydoxylamine hydrochloride

: 136943-84-5
O-benzyl-N-isopropylhydroxylamine

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / H₂SO₄ / 10 h / Heating

2: 72 percent / NaCNBH₃; HCl / methanol / 20 h

With hydrogenchloride; sulfuric acid; sodium cyanoborohydride; In methanol; 1: Condensation / 2: Reduction;

Reference yield:

: 2687-43-6
O-benzylhydoxylamine hydrochloride

: 136943-84-5
O-benzyl-N-isopropylhydroxylamine

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium acetate / water; methanol / 12 h / 20 °C

2.1: sodium cyanoborohydride / ethanol / 0.25 h / 0 °C

2.2: 0 °C

With sodium acetate; sodium cyanoborohydride; In methanol; ethanol; water;
DOI:10.1021/jacs.0c07600