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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
Structure of Dibenzyl phosphate

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)

HIDE SMILES / InChI

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

PubMed

TitleDatePubMed
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 Mon Mar 31 21:54:45 GMT 2025
Edited
by admin
on Mon Mar 31 21:54:45 GMT 2025
Record UNII
Y65R35LZ0S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Dibenzyl phosphate
Systematic Name English
Benzyl phosphate, OP(OCH<sub>2</sub>Ph)<sub>2</sub>OH
Preferred Name English
Dibenzyl hydrogen phosphate
Systematic Name English
Phosphoric acid, bis(phenylmethyl) ester
Systematic Name English
Phosphoric acid, dibenzyl ester
Systematic Name English
Dibenzylphosphoric acid
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
216-602-3
Created by admin on Mon Mar 31 21:54:45 GMT 2025 , Edited by admin on Mon Mar 31 21:54:45 GMT 2025
PRIMARY
CAS
1623-08-1
Created by admin on Mon Mar 31 21:54:45 GMT 2025 , Edited by admin on Mon Mar 31 21:54:45 GMT 2025
PRIMARY
EPA CompTox
DTXSID1033402
Created by admin on Mon Mar 31 21:54:45 GMT 2025 , Edited by admin on Mon Mar 31 21:54:45 GMT 2025
PRIMARY
PUBCHEM
74189
Created by admin on Mon Mar 31 21:54:45 GMT 2025 , Edited by admin on Mon Mar 31 21:54:45 GMT 2025
PRIMARY
FDA UNII
Y65R35LZ0S
Created by admin on Mon Mar 31 21:54:45 GMT 2025 , Edited by admin on Mon Mar 31 21:54:45 GMT 2025
PRIMARY
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