N-(Acetyloxy)-N-(prop-2-en-1-yl)hex-5-enamide

Base Information

Chemical Name:N-(Acetyloxy)-N-(prop-2-en-1-yl)hex-5-enamide
CAS No.:77413-80-0
Molecular Formula:C₁₁H₁₇NO₃
Molecular Weight:211.261
Hs Code.:
DSSTox Substance ID:DTXSID00507625
Wikidata:Q82363941

Synonyms:77413-80-0;N-(Acetyloxy)-N-(prop-2-en-1-yl)hex-5-enamide;DTXSID00507625

Suppliers and Price of N-(Acetyloxy)-N-(prop-2-en-1-yl)hex-5-enamide

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 N-(Acetyloxy)-N-(prop-2-en-1-yl)hex-5-enamide

Chemical Property:

XLogP3:1.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:8
Exact Mass:211.12084340
Heavy Atom Count:15
Complexity:248

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)ON(CC=C)C(=O)CCCC=C

Technology Process of N-(Acetyloxy)-N-(prop-2-en-1-yl)hex-5-enamide

There total 2 articles about N-(Acetyloxy)-N-(prop-2-en-1-yl)hex-5-enamide 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: 86.0%

: 36394-07-7
5-hexenoyl chloride

: 87842-66-8
O-acetyl-N-allylhydroxylamine

: 77413-80-0
N-5-hexenoyl-N-allyl-O-acetylhydroxylamine

Guidance literature:: With triethylamine; In tetrachloromethane; for 1h; Ambient temperature;
DOI:10.1021/ja00364a040

Reference yield:

: 87842-65-7
N,O-diacetyl-1-allylhydroxylamine

: 77413-80-0
N-5-hexenoyl-N-allyl-O-acetylhydroxylamine

Guidance literature:: Multi-step reaction with 2 steps

1: 54 percent / 6N HCl / H₂O / 1 h / Ambient temperature

2: 86 percent / Et₃N / CCl₄ / 1 h / Ambient temperature

With hydrogenchloride; triethylamine; In tetrachloromethane; water;
DOI:10.1021/ja00364a040