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chlorphenesin carbamate

CAS 886-74-8C10H12ClNO4MW 245.66

chlorphenesin carbamate (CAS 886-74-8) — formula C10H12ClNO4, molecular weight 245.66; category organic chemicals.

Product Overview

CAS Number886-74-8
Molecular FormulaC10H12ClNO4
Molecular Weight245.66
Melting Point89-91 °C
LogP1.2
ApplicationsUses: MEDICATION, MEDICATION (VET):, Use Classification: Animal Drugs -> FDA Approved Animal Drug Products (Green Book) -> Active Ingredients, Methods of Manufacturing: ADDITION OF P-CHLOROPHENOL TO 2, 3-EPOXY-1-PROPANOL IN THE PRESENCE OF A TERTIARY AMINE CATALYST FOLLOWED BY TREATMENT OF THE RESULTING 3-(P-CHLOROPHENOXY)-1, 2-PROPANEDIOL WITH CARBAMOYL CHLORIDE, COLLINS, MATTHEWS, PARKER, US PATENTS 3, 161, 567, 3, 214, 336 (1964, 1965, BOTH TO UPJOHN)., CHLOROPHENOL IS CAUSED TO UNDERGO ADDITION TO GLYCIDOL (2, 3-EPOXY-1-PROPANOL) BY CATALYTIC INFLUENCE OF TERTIARY AMINE TO FORM 3-(P-CHLOROPHENOXY)-1, 2-PROPANEDIOL & 1-HYDROXY GROUP IS THEN ESTERIFIED BY REACTION WITH CARBAMOYL CHLORIDE., Consumption Patterns: PROBABLY 100% AS SKELETAL MUSCLE RELAXANT (1975), U.S. Production: (1972) PROBABLY GREATER THAN 4.54X10+5 GRAMS, (1975) PROBABLY GREATER THAN 4.54X10+5 GRAMS, U.S. Imports: (1972) No Data, (1975) No Data, U.S. Exports: (1972) No Data
CategoryOrganic Chemicals

Applications

Documented applications: Uses: MEDICATION, MEDICATION (VET):, Use Classification: Animal Drugs -> FDA Approved Animal Drug Products (Green Book) -> Active Ingredients, Methods of Manufacturing: ADDITION OF P-CHLOROPHENOL TO 2, 3-EPOXY-1-PROPANOL IN THE PRESENCE OF A TERTIARY AMINE CATALYST FOLLOWED BY TREATMENT OF THE RESULTING 3-(P-CHLOROPHENOXY)-1, 2-PROPANEDIOL WITH CARBAMOYL CHLORIDE, COLLINS, MATTHEWS, PARKER, US PATENTS 3, 161, 567, 3, 214, 336 (1964, 1965, BOTH TO UPJOHN)., CHLOROPHENOL IS CAUSED TO UNDERGO ADDITION TO GLYCIDOL (2, 3-EPOXY-1-PROPANOL) BY CATALYTIC INFLUENCE OF TERTIARY AMINE TO FORM 3-(P-CHLOROPHENOXY)-1, 2-PROPANEDIOL & 1-HYDROXY GROUP IS THEN ESTERIFIED BY REACTION WITH CARBAMOYL CHLORIDE., Consumption Patterns: PROBABLY 100% AS SKELETAL MUSCLE RELAXANT (1975), U.S. Production: (1972) PROBABLY GREATER THAN 4.54X10+5 GRAMS, (1975) PROBABLY GREATER THAN 4.54X10+5 GRAMS, U.S. Imports: (1972) No Data, (1975) No Data, U.S. Exports: (1972) No Data.

Technical Profile

What this product is

chlorphenesin carbamate is a carbon-based organic compound with CAS registry number 886-74-8 and molecular formula C10H12ClNO4 (molecular weight 245.66), belonging to the organic chemicals segment of chemical raw materials.

Identification

CAS number: 886-74-8

Its molecular formula C10H12ClNO4 comprises 10 C, 12 H, 1 Cl, 1 N, 4 O atoms.

Also known as: chlorphenesin carbamate · 氯苯甘醚氨基甲酸酯

Category: organic chemicals

Frequently Asked Questions

What is the CAS number of chlorphenesin carbamate?

The CAS registry number of chlorphenesin carbamate is 886-74-8.

What is the molecular formula and molecular weight of chlorphenesin carbamate?

Molecular formula C10H12ClNO4, molecular weight 245.66.

What other names is chlorphenesin carbamate known by?

It is also registered under: chlorphenesin carbamate, 氯苯甘醚氨基甲酸酯.

What are the documented applications of chlorphenesin carbamate?

Recorded applications: Uses: MEDICATION, MEDICATION (VET):, Use Classification: Animal Drugs -> FDA Approved Animal Drug Products (Green Book) -> Active Ingredients, Methods of Manufacturing: ADDITION OF P-CHLOROPHENOL TO 2, 3-EPOXY-1-PROPANOL IN THE PRESENCE OF A TERTIARY AMINE CATALYST FOLLOWED BY TREATMENT OF THE RESULTING 3-(P-CHLOROPHENOXY)-1, 2-PROPANEDIOL WITH CARBAMOYL CHLORIDE, COLLINS, MATTHEWS, PARKER, US PATENTS 3, 161, 567, 3, 214, 336 (1964, 1965, BOTH TO UPJOHN)., CHLOROPHENOL IS CAUSED TO UNDERGO ADDITION TO GLYCIDOL (2, 3-EPOXY-1-PROPANOL) BY CATALYTIC INFLUENCE OF TERTIARY AMINE TO FORM 3-(P-CHLOROPHENOXY)-1, 2-PROPANEDIOL & 1-HYDROXY GROUP IS THEN ESTERIFIED BY REACTION WITH CARBAMOYL CHLORIDE., Consumption Patterns: PROBABLY 100% AS SKELETAL MUSCLE RELAXANT (1975), U.S. Production: (1972) PROBABLY GREATER THAN 4.54X10+5 GRAMS, (1975) PROBABLY GREATER THAN 4.54X10+5 GRAMS, U.S. Imports: (1972) No Data, (1975) No Data, U.S. Exports: (1972) No Data.

Which category does chlorphenesin carbamate belong to?

Category: Organic Chemicals.

PubChem Public Data

Independent reference data for chlorphenesin carbamate (CAS 886-74-8), compiled from public chemistry databases.

Registry identifiers across databases

CAS Registry Number886-74-8
PubChem CID2724
Molecular formulaC10H12ClNO4
IUPAC name[3-(4-chlorophenoxy)-2-hydroxypropyl] carbamate
UNII (FDA)57U5YI11WP

Computed descriptors

Molecular Weight245.66
XLogP31.2
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count6
Exact Mass245.0454856
Monoisotopic Mass245.0454856
Topological Polar Surface Area81.8
Heavy Atom Count16

Physicochemical values on record

Melting Point89-91 °C

Documented uses on record

    Animal Drugs -> FDA Approved Animal Drug Products (Green Book) -> Active IngredientsADDITION OF P-CHLOROPHENOL TO 2,3-EPOXY-1-PROPANOL IN THE PRESENCE OF A TERTIARY AMINE CATALYST FOLLOWED BY TREATMENT OF THE RESULTING 3-(P-CHLOROPHENOXY)-1,2-PROPANEDIOL WITH CARBAMOYL CHLORIDE

    Synonyms and trade names

    CHLORPHENESIN CARBAMATE; 886-74-8; Maolate; Rinlaxer; 3-(4-Chlorophenoxy)-2-hydroxypropyl carbamate; 3-(p-Chlorophenoxy)-1,2-propanediol 1-carbamate; 3-(p-Chlorophenoxy)-2-hydroxypropyl carbamate; 3-(4-Chlorophenoxy)-1,2-propanediol-1-carbamate; DTXSID5022803; U-19,646; 3-(p-Chlorophenoxy)-1,2-propanediol-1-carbamate; U 19646; 1,2-Propanediol, 3-(p-chlorophenoxy)-, 1-carbamate; NSC-82943; carbamic acid 3-(p-chlorophenoxy)-2-hydroxypropyl ester; 57U5YI11WP

    What the public record says

    chlorphenesin carbamate · CAS 886-74-8 · C10H12ClNO4. UNII 57U5YI11WP. Melting Point: 89-91 °C.

    Physical description and handling notes

    Source: PubChem / Wikidata; the batch COA governs where values differ.

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