Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H14O4P.Na |
| Molecular Weight | 300.2221 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].[O-]P(=O)(OCC1=CC=CC=C1)OCC2=CC=CC=C2
InChI
InChIKey=QUFBGLCLSVONQA-UHFFFAOYSA-M
InChI=1S/C14H15O4P.Na/c15-19(16,17-11-13-7-3-1-4-8-13)18-12-14-9-5-2-6-10-14;/h1-10H,11-12H2,(H,15,16);/q;+1/p-1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Quinone methide phosphodiester alkylations under aqueous conditions. | 2001 Oct 19 |
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| Biosynthetic studies on the alpha-glucosidase inhibitor acarbose: the chemical synthesis of dTDP-4-amino-4,6-dideoxy-alpha-D-glucose. | 2002 Feb 18 |
|
| Synthesis of GDP-5-thiosugars and their use as glycosyl donor substrates for glycosyltransferases. | 2003 Aug 8 |
|
| A chemical synthesis of UDP-LacNAc and its regioisomer for finding 'oligosaccharide transferases'. | 2006 Nov |
|
| Lewis acid mediated regioselective ring opening of benzylglycidol with dibenzyl phosphate: Short and attractive synthesis of dihydroxyacetone phosphate. | 2006 Sep 14 |
|
| Synthesis of phosphate derivatives related to the glycosidase inhibitor salacinol. | 2007 Sep 3 |
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3784Q73FLM
Created by
admin on Sat Dec 16 07:10:52 GMT 2023 , Edited by admin on Sat Dec 16 07:10:52 GMT 2023
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23666572
Created by
admin on Sat Dec 16 07:10:52 GMT 2023 , Edited by admin on Sat Dec 16 07:10:52 GMT 2023
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97174-13-5
Created by
admin on Sat Dec 16 07:10:52 GMT 2023 , Edited by admin on Sat Dec 16 07:10:52 GMT 2023
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PARENT (SALT/SOLVATE)
SUBSTANCE RECORD
