U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C8H11Cl3O6
Molecular Weight 309.528
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of .BETA.-CHLORALOSE

SMILES

OC[C@@H](O)[C@H]1O[C@@H]2O[C@H](O[C@@H]2[C@H]1O)C(Cl)(Cl)Cl

InChI

InChIKey=OJYGBLRPYBAHRT-GVUNPQSCSA-N
InChI=1S/C8H11Cl3O6/c9-8(10,11)7-16-5-3(14)4(2(13)1-12)15-6(5)17-7/h2-7,12-14H,1H2/t2-,3+,4-,5-,6-,7+/m1/s1

HIDE SMILES / InChI
Molecular Formula C8H11Cl3O6
Molecular Weight 309.528
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 6 / 6
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: The description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/20488435 | https://www.ncbi.nlm.nih.gov/pubmed/13815011 | https://www.ncbi.nlm.nih.gov/pubmed/926025

Beta-Chloralose is a derivative of chloral hydrate that was used as building block in organic chemistry. Chloralose is prepared by heating equal quantities of glucose and chloral hydrate under controlled conditions so that two isomers are produced. Only alpha-chloralose has narcotic properties, beta-chloralose can produce muscular pain.

Originator

Richet, C.
2
Sources: Un nouvel hypnotique; le chloralose. Revue Scientifique, 1893, Paris: 51:175-178. 354.

Approval Year

Unknown
149124
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Synthesis and antimicrobial activities of two novel amino sugars derived from chloraloses.
2010-07-19
Patents

Patents

SU287918
1

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:05:59 GMT 2025
Edited
by admin
on Mon Mar 31 22:05:59 GMT 2025
Record UNII
7CUN2U7N0Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
.BETA.-CHLORALOSE
Common Name English
NSC-52806
Preferred Name English
.ALPHA.-D-GLUCOFURANOSE, 1,2-O-((1S)-2,2,2-TRICHLOROETHYLIDENE)-CHLORALOSE, .BETA.-
Systematic Name English
Code System Code Type Description
FDA UNII
7CUN2U7N0Q
Created by admin on Mon Mar 31 22:05:59 GMT 2025 , Edited by admin on Mon Mar 31 22:05:59 GMT 2025
PRIMARY
PUBCHEM
5284343
Created by admin on Mon Mar 31 22:05:59 GMT 2025 , Edited by admin on Mon Mar 31 22:05:59 GMT 2025
PRIMARY
NSC
52806
Created by admin on Mon Mar 31 22:05:59 GMT 2025 , Edited by admin on Mon Mar 31 22:05:59 GMT 2025
PRIMARY
EPA CompTox
DTXSID4046575
Created by admin on Mon Mar 31 22:05:59 GMT 2025 , Edited by admin on Mon Mar 31 22:05:59 GMT 2025
PRIMARY
CAS
16376-36-6
Created by admin on Mon Mar 31 22:05:59 GMT 2025 , Edited by admin on Mon Mar 31 22:05:59 GMT 2025
PRIMARY
ECHA (EC/EINECS)
240-429-2
Created by admin on Mon Mar 31 22:05:59 GMT 2025 , Edited by admin on Mon Mar 31 22:05:59 GMT 2025
PRIMARY
NIH
NCATS
PRIVACY NOTICE
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966