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
SMILES
[H][C@@]1(O[C@]2([H])O[C@H](O[C@]2([H])[C@H]1O)C(Cl)(Cl)Cl)[C@H](O)CO
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
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 |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/13936089Curator'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
Sources: https://www.ncbi.nlm.nih.gov/pubmed/13936089
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.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:28:24 GMT 2023
by
admin
on
Sat Dec 16 08:28:24 GMT 2023
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Record UNII |
7CUN2U7N0Q
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Record Status |
Validated (UNII)
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Record Version |
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