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Details

Stereochemistry RACEMIC
Molecular Formula C5H8Cl3NO3
Molecular Weight 236.481
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARBOCLORAL

SMILES

CCOC(=O)NC(O)C(Cl)(Cl)Cl

InChI

InChIKey=ITMSAWKLJVGBIT-UHFFFAOYSA-N
InChI=1S/C5H8Cl3NO3/c1-2-12-4(11)9-3(10)5(6,7)8/h3,10H,2H2,1H3,(H,9,11)

HIDE SMILES / InChI

Molecular Formula C5H8Cl3NO3
Molecular Weight 236.481
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Carbocloral is a carbamate ester derivative used as sedative and hypnotic drug. Carbocloral is as effective as chloral hydrate in producing sedation, hypnosis, and general anesthesia, and more effective in inducing relaxation of skeletal muscles. Carbocloral was also more effective as an anticonvulsant and less toxic than chloral hydrate.

Originator

Sources: Journal fuer Praktische Chemie (Leipzig) 41, (2), 266-77. From: J. Chem. Soc., Abstr. 58, 571-2 1890.

Approval Year

PubMed

PubMed

TitleDatePubMed
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:31:40 GMT 2023
Edited
by admin
on Sat Dec 16 16:31:40 GMT 2023
Record UNII
K0KA807799
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CARBOCLORAL
INN   MI   USAN  
USAN   INN  
Official Name English
CN-16146
Code English
carbocloral [INN]
Common Name English
CARBAMIC ACID, (2,2,2-TRICHLORO-1-HYDROXYETHYL)-, ETHYL ESTER
Common Name English
CARBOCLORAL [MI]
Common Name English
HY-185
Code English
CI-336
Code English
Ethyl (2,2,2-trichloro-1-hydroxyethyl)carbamate
Systematic Name English
CARBOCLORAL [USAN]
Common Name English
PRODORM
Brand Name English
NSC-33077
Code English
Classification Tree Code System Code
NCI_THESAURUS C29756
Created by admin on Sat Dec 16 16:31:40 GMT 2023 , Edited by admin on Sat Dec 16 16:31:40 GMT 2023
Code System Code Type Description
SMS_ID
100000084585
Created by admin on Sat Dec 16 16:31:40 GMT 2023 , Edited by admin on Sat Dec 16 16:31:40 GMT 2023
PRIMARY
NSC
33077
Created by admin on Sat Dec 16 16:31:40 GMT 2023 , Edited by admin on Sat Dec 16 16:31:40 GMT 2023
PRIMARY
NCI_THESAURUS
C65287
Created by admin on Sat Dec 16 16:31:40 GMT 2023 , Edited by admin on Sat Dec 16 16:31:40 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104032
Created by admin on Sat Dec 16 16:31:40 GMT 2023 , Edited by admin on Sat Dec 16 16:31:40 GMT 2023
PRIMARY
DRUG CENTRAL
3701
Created by admin on Sat Dec 16 16:31:40 GMT 2023 , Edited by admin on Sat Dec 16 16:31:40 GMT 2023
PRIMARY
EVMPD
SUB06611MIG
Created by admin on Sat Dec 16 16:31:40 GMT 2023 , Edited by admin on Sat Dec 16 16:31:40 GMT 2023
PRIMARY
FDA UNII
K0KA807799
Created by admin on Sat Dec 16 16:31:40 GMT 2023 , Edited by admin on Sat Dec 16 16:31:40 GMT 2023
PRIMARY
PUBCHEM
10944
Created by admin on Sat Dec 16 16:31:40 GMT 2023 , Edited by admin on Sat Dec 16 16:31:40 GMT 2023
PRIMARY
MERCK INDEX
m621
Created by admin on Sat Dec 16 16:31:40 GMT 2023 , Edited by admin on Sat Dec 16 16:31:40 GMT 2023
PRIMARY Merck Index
CAS
541-79-7
Created by admin on Sat Dec 16 16:31:40 GMT 2023 , Edited by admin on Sat Dec 16 16:31:40 GMT 2023
PRIMARY
EPA CompTox
DTXSID9046233
Created by admin on Sat Dec 16 16:31:40 GMT 2023 , Edited by admin on Sat Dec 16 16:31:40 GMT 2023
PRIMARY
INN
2184
Created by admin on Sat Dec 16 16:31:40 GMT 2023 , Edited by admin on Sat Dec 16 16:31:40 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY