Carbamic acid, 1-propenyl-, 1,1-dimethylethyl ester (9CI)

Base Information

Chemical Name:Carbamic acid, 1-propenyl-, 1,1-dimethylethyl ester (9CI)
CAS No.:131971-64-7
Molecular Formula:C8H15 N O2
Molecular Weight:157.2102
Hs Code.:
Mol file:131971-64-7.mol

Synonyms:Carbamicacid, 1-propenyl-, 1,1-dimethylethyl ester (9CI); tert-Butyl(1-propenyl)carbamate

Suppliers and Price of Carbamic acid, 1-propenyl-, 1,1-dimethylethyl ester (9CI)

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 1 raw suppliers

Chemical Property of Carbamic acid, 1-propenyl-, 1,1-dimethylethyl ester (9CI)

Chemical Property:

PSA：38.33000
LogP:2.43560

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Carbamic acid, 1-propenyl-, 1,1-dimethylethyl ester (9CI)

There total 10 articles about Carbamic acid, 1-propenyl-, 1,1-dimethylethyl ester (9CI) 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: 98.0%

: 78888-18-3
N-tert-butoxycarbonylprop-2-en-1-amine

: 131971-64-7
1-[(tert-butoxycarbonyl)amino]prop-1-ene

Guidance literature:: With rhodium hydrido (PEt₃)3 complex; In tetrahydrofuran; at 100 ℃; for 6h;
DOI:10.1039/c39900001304

Reference yield: 78.0%

: 2592-18-9,23082-29-3,55674-67-4,85979-33-5,86748-77-8,23082-30-6
N-tert-butoxycarbonyl-L-allo-threonine

: 119973-54-5,131971-64-7,119973-55-6
(Z)-1-<(tert-butoxycarbonyl)amino>propene

Guidance literature:: With dimethyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; 1.) -78 deg C, 20 min, 2.) 25 deg C, 1.5 h;
DOI:10.1021/jo00271a013

Reference yield: 78.0%

: 67-56-1
methanol

: 78888-18-3
N-tert-butoxycarbonylprop-2-en-1-amine

: 131971-64-7
1-[(tert-butoxycarbonyl)amino]prop-1-ene

: 131971-61-4
(1-Methoxy-propyl)-carbamic acid tert-butyl ester

Guidance literature:: With rhodium hydrido (PEt₃)3 complex; at 65 ℃; for 12h; Product distribution; Mechanism; var. reaction conditions; other alcohol and N-tert-butoxycarbonyl allylamines;
DOI:10.1039/c39900001304