Chlorphenesin carbamate

Base Information

Chemical Name:Chlorphenesin carbamate
CAS No.:886-74-8
Molecular Formula:C₁₀H₁₂ClNO₄
Molecular Weight:245.663
Hs Code.:
European Community (EC) Number:212-954-7
NSC Number:82943
UNII:57U5YI11WP,HQC4WI89YG,G014XC07GH
DSSTox Substance ID:DTXSID5022803
Nikkaji Number:J7.158G
Wikipedia:Chlorphenesin_carbamate
Wikidata:Q27106156
NCI Thesaurus Code:C65322
Metabolomics Workbench ID:53066
ChEMBL ID:CHEMBL607710
Mol file:886-74-8.mol

Synonyms:chlorphenesin carbamate

Suppliers and Price of Chlorphenesin carbamate

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

Medical Isotopes, Inc.
Chlorphenesincarbamate
1 g
$ 580.00

American Custom Chemicals Corporation
CHLORPHENESIN CARBAMATE 95.00%
500G
$ 4984.40

AHH
Chlorphenesincarbamate 99%
500g
$ 540.00

Total 41 raw suppliers

Chemical Property of Chlorphenesin carbamate

Chemical Property:

Vapor Pressure:4.28E-10mmHg at 25°C
Melting Point:89-91°
Refractive Index:1.6000 (estimate)
Boiling Point:481.8°C at 760 mmHg
Flash Point:245.2°C
PSA：81.78000
Density:1.365g/cm³
LogP:1.87530
Storage Temp.:-20°C, Inert atmosphere
Solubility.:DMSO (Slightly), Methanol (Slightly)
XLogP3:1.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:245.0454856
Heavy Atom Count:16
Complexity:219

Purity/Quality:

99% ^*data from raw suppliers

Chlorphenesincarbamate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1OCC(COC(=O)N)O)Cl
Uses Maolate is a pharmaceutical compound comprising naproxen. 'Muscle relaxant
Therapeutic Function Muscle relaxant

Technology Process of Chlorphenesin carbamate

There total 2 articles about Chlorphenesin carbamate 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:

: 61514-96-3
3-(p-chlorophenoxy)-1,2-propanediol-2-carbamate

: 886-74-8,126632-50-6
chlorphenesin carbamate

: 104-29-0
chlorphenesin

Guidance literature:: With sodium hydroxide; In water; at 0 ℃; Rate constant; degradation was studied;
DOI:10.1248/cpb.34.1764

Reference yield:

: 886-74-8,126632-50-6
chlorphenesin carbamate

Guidance literature:: COCl2, 3-p-Chlorophenoxy-1.2-propandiol, NH4OH;

Reference yield: 63.0%

: 886-74-8,126632-50-6
chlorphenesin carbamate

: 3-(4-chloro-2-hydroxyphenoxy)-2-hydroxypropyl carbamate

Guidance literature:: chlorphenesin carbamate; With 4,5-dichlorophthalic anhydride; 6,7-dichlorobenzo[d][1,2]dioxine-1,4-dione; In chloroform; at 50 ℃; for 24h;

With water; sodium hydrogencarbonate; In methanol; at 50 ℃; for 1h; regioselective reaction; Inert atmosphere;
DOI:10.1021/acs.joc.5b01079