Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H15O4P |
| Molecular Weight | 278.2403 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OP(=O)(OCC1=CC=CC=C1)OCC2=CC=CC=C2
InChI
InChIKey=HDFFVHSMHLDSLO-UHFFFAOYSA-N
InChI=1S/C14H15O4P/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)
| Molecular Formula | C14H15O4P |
| Molecular Weight | 278.2403 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis of phosphate derivatives related to the glycosidase inhibitor salacinol. | 2007-09-03 |
|
| A chemical synthesis of UDP-LacNAc and its regioisomer for finding 'oligosaccharide transferases'. | 2006-11 |
|
| Lewis acid mediated regioselective ring opening of benzylglycidol with dibenzyl phosphate: Short and attractive synthesis of dihydroxyacetone phosphate. | 2006-09-14 |
|
| Synthesis of GDP-5-thiosugars and their use as glycosyl donor substrates for glycosyltransferases. | 2003-08-08 |
|
| Biosynthetic studies on the alpha-glucosidase inhibitor acarbose: the chemical synthesis of dTDP-4-amino-4,6-dideoxy-alpha-D-glucose. | 2002-02-18 |
|
| Quinone methide phosphodiester alkylations under aqueous conditions. | 2001-10-19 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:54:45 GMT 2025
by
admin
on
Mon Mar 31 21:54:45 GMT 2025
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| Record UNII |
Y65R35LZ0S
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| Record Status |
Validated (UNII)
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| Record Version |
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216-602-3
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1623-08-1
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DTXSID1033402
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74189
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Y65R35LZ0S
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admin on Mon Mar 31 21:54:45 GMT 2025 , Edited by admin on Mon Mar 31 21:54:45 GMT 2025
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