Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C3H6O2 |
Molecular Weight | 74.0785 |
Optical Activity | ( - ) |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@H](O)C=O
InChI
InChIKey=BSABBBMNWQWLLU-VKHMYHEASA-N
InChI=1S/C3H6O2/c1-3(5)2-4/h2-3,5H,1H3/t3-/m0/s1
Molecular Formula | C3H6O2 |
Molecular Weight | 74.0785 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Physiological basis for rhamnose utilization by a mutant of Pasteurella pestis. I. Experiments with resting cells; the isolation of lactic aldehyde. | 1957 Jul |
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Studies on the metabolism of lactaldehyde. I. Separation and determination of lactaldehyde and related 3-carbon compounds. | 1958 Jan |
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THE METABOLISM OF LACTALDEHYDE. VII. THE OXIDATION OF D-LACTALDEHYDE IN RAT LIVER. | 1965 Mar 8 |
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L-Rhamnose utilisation in Salmonella typhimurium. | 1984 Apr |
|
Constitutive activation of L-fucose genes by an unlinked mutation in Escherichia coli. | 1984 Aug |
|
The metabolism of acetone in rat. | 1984 Jan 10 |
|
Crystal structure of lactaldehyde dehydrogenase from Escherichia coli and inferences regarding substrate and cofactor specificity. | 2007 Feb 16 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:53:42 GMT 2023
by
admin
on
Sat Dec 16 11:53:42 GMT 2023
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Record UNII |
BS76EN9C35
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Record Status |
Validated (UNII)
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Record Version |
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-
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439231
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3913-64-2
Created by
admin on Sat Dec 16 11:53:42 GMT 2023 , Edited by admin on Sat Dec 16 11:53:42 GMT 2023
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18041
Created by
admin on Sat Dec 16 11:53:42 GMT 2023 , Edited by admin on Sat Dec 16 11:53:42 GMT 2023
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BS76EN9C35
Created by
admin on Sat Dec 16 11:53:42 GMT 2023 , Edited by admin on Sat Dec 16 11:53:42 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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RACEMATE -> ENANTIOMER |
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