CHLORPHENESIN CARBAMATE

  • Name: CHLORPHENESIN CARBAMATE
  • CAS: 886-74-8
  • Purity: 99%
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1.What is the CHLORPHENESIN CARBAMATE ?

'Muscle relaxant

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

3-(p-chlorophenoxy)-1,2-propanediol-2-carbamate

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

chlorphenesin carbamate

chlorphenesin
104-29-0

chlorphenesin

Conditions
Conditions Yield
With sodium hydroxide; In water; at 0 ℃; Rate constant; degradation was studied;
chlorphenesin carbamate
886-74-8,126632-50-6

chlorphenesin carbamate

Conditions
Conditions Yield
COCl2, 3-p-Chlorophenoxy-1.2-propandiol, NH4OH;

2.What is the CAS number for CHLORPHENESIN CARBAMATE ?

The CAS number of CHLORPHENESIN CARBAMATE is 886-74-8.

More information of CHLORPHENESIN CARBAMATE 886-74-8 are:

CAS?Number

886-74-8

Density

1.365g/cm3

Melting Point

89-91°

Boiling Point

481.8°C at 760 mmHg

Flash Point

245.2°C

Vapor Pressure

4.28E-10mmHg at 25°C

Refractive Index

1.6000 (estimate)

PSA

81.78000

LogP

1.87530

3.What are another words for CHLORPHENESIN CARBAMATE ?

Synonyms?for?CHLORPHENESIN CARBAMATE 886-74-8:1,2-Propanediol,3-(p-chlorophenoxy)-, 1-carbamate (8CI); Carbamic acid,3-(p-chlorophenoxy)-2-hydroxypropyl ester (7CI);3-(4-Chlorophenoxy)-2-hydroxypropyl carbamate;3-(p-Chlorophenoxy)-2-hydroxypropyl carbamate;3-[p-Chlorophenoxy]-1,2-propanediol-1-carbamate; Chlorphenesin carbamate;Maolate; NSC 82943; Rinlaxer; U 19646; U-19,646

4.What is the molecular formula of CHLORPHENESIN CARBAMATE?

The chemical formula of ?CHLORPHENESIN CARBAMATE is?C10 H12 ClNO4 which containing 10 Carbon atoms,12 Hydrogen atoms,1 Chlorine atoms,1 Nitrogen atoms and 4 Oxygen atoms,and the molecular weight of??CHLORPHENESIN CARBAMATE?is 245.663.

5.What is CHLORPHENESIN CARBAMATE (886-74-8) used for?

Chlorphenesin Carbamate, also known as Maolate, is a pharmaceutical compound derived from the lead compound mephenesin. It is a p-chloro substituted and 1-carbamate derivative that exhibits increased activity and lipophilicity due to p-chlorination and carbamylation of the primary hydroxyl group. This modification results in a centrally acting skeletal muscle relaxant with a biological half-life of 3.5 hours in humans.

InChI:InChI=1/C10H12ClNO4/c11-7-1-3-9(4-2-7)15-5-8(13)6-16-10(12)14/h1-4,8,13H,5-6H2,(H2,12,14)

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