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About This Item
Linear Formula:
(C6H5CH2O)2P(O)(OH)
CAS Number:
Molecular Weight:
278.24
Beilstein:
2055755
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
99%
form
powder
mp
78-80 °C (lit.)
storage temp.
2-8°C
SMILES string
OP(=O)(OCc1ccccc1)OCc2ccccc2
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)
InChI key
HDFFVHSMHLDSLO-UHFFFAOYSA-N
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Application
Dibenzyl phosphate (DBzP) can be used:
- To promote the monoselective ortho-C-H alkylation of N-quinolyl benzamides with primary and secondary alkyl iodides.
- For the ring-opening reaction of epoxide such as benzylglycidol to synthesize dihydroxyacetone phosphate (DHAP).
- As a reactant for the synthesis of stereospecific 1,2-trans glycosyl phosphates.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Syntheses of glycosyl phosphates by phase transfer catalysis.
Roy R, et al.
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Lewis acid mediated regioselective ring opening of benzylglycidol with dibenzyl phosphate: short and attractive synthesis of dihydroxyacetone phosphate.
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