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Details

Stereochemistry EPIMERIC
Molecular Formula C13H11O6.Na
Molecular Weight 286.2126
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SODIUM 5,6-BENZYLIDENEASCORBATE

SMILES

[Na+].OC1=C([O-])[C@H](OC1=O)[C@@H]2COC(O2)C3=CC=CC=C3

InChI

InChIKey=JLUAVHQVEFDQEO-ZKZAMAJLSA-M
InChI=1S/C13H12O6.Na/c14-9-10(15)12(16)19-11(9)8-6-17-13(18-8)7-4-2-1-3-5-7;/h1-5,8,11,13-15H,6H2;/q;+1/p-1/t8-,11+,13?;/m0./s1

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Sodium benzylideneascorbate induces apoptosis in HIV-replicating U1 cells.
1994-08-29
Patents
Name Type Language
SODIUM 5,6-BENZYLIDENEASCORBATE
Common Name English
L-ASCORBIC ACID, 5,6-O-(PHENYLMETHYLENE)-, MONOSODIUM SALT
Preferred Name English
L-ASCORBIC ACID, 5,6-O-(PHENYLMETHYLENE)-, SODIUM SALT (1:1)
Common Name English
SODIUM 5,6-BENZYLIDENE-L-ASCORBATE
Common Name English
Code System Code Type Description
CAS
98734-55-5
Created by admin on Mon Mar 31 22:10:59 GMT 2025 , Edited by admin on Mon Mar 31 22:10:59 GMT 2025
PRIMARY
FDA UNII
2M55S7ZFFQ
Created by admin on Mon Mar 31 22:10:59 GMT 2025 , Edited by admin on Mon Mar 31 22:10:59 GMT 2025
PRIMARY
PUBCHEM
71587369
Created by admin on Mon Mar 31 22:10:59 GMT 2025 , Edited by admin on Mon Mar 31 22:10:59 GMT 2025
PRIMARY
EPA CompTox
DTXSID50243788
Created by admin on Mon Mar 31 22:10:59 GMT 2025 , Edited by admin on Mon Mar 31 22:10:59 GMT 2025
PRIMARY