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1708-40-3

1708-40-3 Structure

1708-40-3 Structure
IdentificationBack Directory
[Name]

1,3-O-BENZYLIDENEGLYCEROL
[CAS]

1708-40-3
[Synonyms]

NSC 97343
90.0%(NMR)
2-phenyl-3-dioxan-5-ol
2-PHENYL-1,3-DIOXAN-2-OL
2-PHENYL-1,3-DIOXAN-5-OL
1,3-BENZYLIDENE GLYCEROL
1,3-O-BENZYLIDENEGLYCEROL
2-Phenyl-1,3-dioxinan-5-ol
1,3-Dioxan-5-ol, 2-phenyl-
2-Phenyl-1,3-dioxan-5-ol>
1-O,3-O-Benzylideneglycerol
5-HYDROXY-2-PHENYL-1,3-DIOXANE
(2r,5r)-2-phenyl-1,3-dioxan-5-ol
purum,mixtureofcis-andtrans-isomeres
Benzaldehyde cyclic 2-hydroxytrimethylene acetal
2-Phenyl-1,3-dioxan-5-ol mixture of cis and trans
1,3-O-BENZYLIDENEGLYCEROL, MIXTURE OF CI S AND TRANS
2-PHENYL-1,3-DIOXAN-5-OL MIXTURE OF CIS AND TRANS 97+%
1,3-O-Benzylideneglycerol 5-Hydroxy-2-phenyl-1,3-dioxane
2-PHENYL-1,3-DIOXAN-5-OL PURUM MIXTURE OF CIS AND TRANS 97+%
2-Phenyl-1,3-dioxan-5-ol Mixture of cis and trans, >=97.0% (HPLC)
[EINECS(EC#)]

216-963-7
[Molecular Formula]

C10H12O3
[MDL Number]

MFCD00047504
[MOL File]

1708-40-3.mol
[Molecular Weight]

180.2
Chemical PropertiesBack Directory
[Melting point ]

84 °C
[Boiling point ]

165-170 °C(Press: 10 Torr)
[density ]

1.203±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

soluble in Methanol,Acetone
[form ]

powder to crystal
[pka]

13.55±0.40(Predicted)
[color ]

White to Almost white
[BRN ]

84059
[InChI]

InChI=1S/C10H12O3/c11-9-6-12-10(13-7-9)8-4-2-1-3-5-8/h1-5,9-11H,6-7H2
[InChIKey]

BWKDAAFSXYPQOS-UHFFFAOYSA-N
[SMILES]

O1CC(O)COC1C1=CC=CC=C1
[EPA Substance Registry System]

1,3-Dioxan-5-ol, 2-phenyl- (1708-40-3)
Safety DataBack Directory
[Risk Statements ]

22
[Safety Statements ]

22-24/25
[WGK Germany ]

3
[F ]

1-10
[HS Code ]

2932.99.9090
Hazard InformationBack Directory
[Uses]

2-Phenyl-1,3-dioxan-5-ol was used as starting reagent in the synthesis of carbonate of glycerol monomer, 5-benzyloxy-1,3-dioxan-2-one which forms copolymers with ε-caprolactone.
[Definition]

ChEBI: Benzaldehyde glyceryl acetal is a member of dioxanes.
[General Description]

cis-2-phenyl-1,3-dioxan-5-ol reacts with triphenylphosphine-carbon tetrabromide to yield cis-4-bromomethyl-2-phenyl-1,3-dioxolan, its trans-diastereoisomer and trans-5-bromo-2-phenyl-1,3-dioxan.
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