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 | 22.9898 |
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 an antitumor antibiotic, Fostriecin (CI-920). | 2003 Jul 9 |
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Total synthesis and structure confirmation of the annonaceous acetogenins 30(S)-hydroxybullatacin, uvarigrandin a, and 5(R)-uvarigrandin a (narumicin I?). | 2003 Mar 7 |
|
A total synthesis of hydroxylysine in protected form and investigations of the reductive opening of p-methoxybenzylidene acetals. | 2004 Dec 10 |
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Diversity of function in the isocitrate lyase enzyme superfamily: the Dianthus caryophyllus petal death protein cleaves alpha-keto and alpha-hydroxycarboxylic acids. | 2005 Dec 20 |
|
Total synthesis of leustroducsin B. | 2008 Jul 18 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 04:55:30 GMT 2023
by
admin
on
Sat Dec 16 04:55:30 GMT 2023
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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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51209-20-2
Created by
admin on Sat Dec 16 04:55:31 GMT 2023 , Edited by admin on Sat Dec 16 04:55:31 GMT 2023
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DTXSID10199217
Created by
admin on Sat Dec 16 04:55:31 GMT 2023 , Edited by admin on Sat Dec 16 04:55:31 GMT 2023
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12784032
Created by
admin on Sat Dec 16 04:55:31 GMT 2023 , Edited by admin on Sat Dec 16 04:55:31 GMT 2023
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2Y0T6D052J
Created by
admin on Sat Dec 16 04:55:31 GMT 2023 , Edited by admin on Sat Dec 16 04:55:31 GMT 2023
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PRIMARY |