Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C4H4O5.2Na |
| Molecular Weight | 178.0511 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].[Na+].O[C@H](CC([O-])=O)C([O-])=O
InChI
InChIKey=WPUMTJGUQUYPIV-YBBRRFGFSA-L
InChI=1S/C4H6O5.2Na/c5-2(4(8)9)1-3(6)7;;/h2,5H,1H2,(H,6,7)(H,8,9);;/q;2*+1/p-2/t2-;;/m1../s1
| Molecular Formula | Na |
| Molecular Weight | 22.98976928 |
| Charge | 1 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C4H4O5 |
| Molecular Weight | 132.0716 |
| Charge | -2 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Total synthesis of leustroducsin B. | 2008-07-18 |
|
| Diversity of function in the isocitrate lyase enzyme superfamily: the Dianthus caryophyllus petal death protein cleaves alpha-keto and alpha-hydroxycarboxylic acids. | 2005-12-20 |
|
| A total synthesis of hydroxylysine in protected form and investigations of the reductive opening of p-methoxybenzylidene acetals. | 2004-12-10 |
|
| Total synthesis of an antitumor antibiotic, Fostriecin (CI-920). | 2003-07-09 |
|
| Total synthesis and structure confirmation of the annonaceous acetogenins 30(S)-hydroxybullatacin, uvarigrandin a, and 5(R)-uvarigrandin a (narumicin I?). | 2003-03-07 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:25:00 GMT 2025
by
admin
on
Mon Mar 31 21:25:00 GMT 2025
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| Record UNII |
2Y0T6D052J
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| Record Status |
Validated (UNII)
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| Record Version |
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-
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Systematic Name | English | ||
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Preferred Name | English | ||
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Common Name | English |
| Code System | Code | Type | Description | ||
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51209-20-2
Created by
admin on Mon Mar 31 21:25:00 GMT 2025 , Edited by admin on Mon Mar 31 21:25:00 GMT 2025
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DTXSID10199217
Created by
admin on Mon Mar 31 21:25:00 GMT 2025 , Edited by admin on Mon Mar 31 21:25:00 GMT 2025
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12784032
Created by
admin on Mon Mar 31 21:25:00 GMT 2025 , Edited by admin on Mon Mar 31 21:25:00 GMT 2025
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PRIMARY | |||
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2Y0T6D052J
Created by
admin on Mon Mar 31 21:25:00 GMT 2025 , Edited by admin on Mon Mar 31 21:25:00 GMT 2025
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PRIMARY |