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About This Item
Empirical Formula (Hill Notation):
C10H12O3
CAS Number:
Molecular Weight:
180.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
216-963-7
Beilstein/REAXYS Number:
84059
MDL number:
Product Name
2-Phenyl-1,3-dioxan-5-ol, mixture of cis and trans, ≥97.0% (HPLC)
InChI key
BWKDAAFSXYPQOS-UHFFFAOYSA-N
InChI
1S/C10H12O3/c11-9-6-12-10(13-7-9)8-4-2-1-3-5-8/h1-5,9-11H,6-7H2
SMILES string
OC1COC(OC1)c2ccccc2
assay
≥97.0% (HPLC)
form
powder
functional group
ether
hydroxyl
phenyl
storage temp.
2-8°C
Quality Level
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Application
2-Phenyl-1,3-dioxan-5-ol can be used as a starting material in the synthesis of 5-benzyloxy1,3-dioxan-2-one (a carbonate of glycerol monomer). It undergoes ring-opening polymerization with ε-caprolactone in presence of tin(II) 2-ethylhexanoate (Sn(oct)2).
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.
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.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
监管及禁止进口产品
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Nucleophilic substitution in glycerol derivatives. Part VI. Halogenodeoxygenation of 2-phenyl-1, 3-dioxan-5-ol to give 1, 3-dioxans and 1, 3-dioxolans.
Aneja R and Davies AP.
Journal of the Chemical Society. Perkin Transactions 1, 141-145 (1974)
Poly (carbonate ester) s based on units of 6-hydroxyhexanoic acid and glycerol.
Wolinsky JB, et al.
Macromolecules, 40(20), 7065-7068 (2007)
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