Pentyl hydroxycarbamate

Base Information

Chemical Name:Pentyl hydroxycarbamate
CAS No.:590-06-7
Molecular Formula:C6H13NO3
Molecular Weight:147.1723
Hs Code.:2924199090
DSSTox Substance ID:DTXSID00207734
Wikidata:Q83081711

Synonyms:Pentyl hydroxycarbamate;Hydroxycarbamic acid pentyl ester;n-Pentyl N-hydroxycarbamate;CCRIS 5074;590-06-7;BRN 1855227;CARBAMIC ACID, HYDROXY-, PENTYL ESTER;SCHEMBL3899146;DTXSID00207734;LS-49967

Suppliers and Price of Pentyl 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 2 raw suppliers

Chemical Property of Pentyl hydroxycarbamate

Chemical Property:

Vapor Pressure:0.000408mmHg at 25°C
Boiling Point:281.9°Cat760mmHg
PKA:9.31±0.23(Predicted)
Flash Point:124.3°C
PSA：62.05000
Density:1.071g/cm³
LogP:1.49640
XLogP3:1.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:147.08954328
Heavy Atom Count:10
Complexity:95

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCOC(=O)NO

Technology Process of Pentyl hydroxycarbamate

There total 2 articles about Pentyl 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:

: 71-41-0
pentan-1-ol

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

: 590-06-7
N-Hydroxy-carbamidsaeure-pentylester

Guidance literature:: pentan-1-ol; 1,1'-carbonyldiimidazole; In tetrahydrofuran; at 0 - 20 ℃; for 1h; Inert atmosphere; Schlenk technique;

With 1H-imidazole; hydroxylamine hydrochloride; In tetrahydrofuran; at 0 - 20 ℃; for 1h; Inert atmosphere; Schlenk technique;
DOI:10.1021/acs.orglett.6b02724