13468

2-Phenyl-1,3-dioxan-5-ol

mixture of cis and trans, ≥97.0% (HPLC)

• Sinónimos: 1,3-O-Benzylideneglycerol
• Fórmula empírica (notación de Hill): C₁₀H₁₂O₃
• Número de CAS: 1708-40-3
• Peso molecular: 180.20
• Beilstein/REAXYS Number: 84059
• EC Number: 216-963-7
• MDL number: MFCD00047504
• UNSPSC Code: 12352100
• PubChem Substance ID: 57647095
• NACRES: NA.22

Propiedades

• assay: ≥97.0% (HPLC)
• form: powder
• functional group: ether
• storage temp.: 2-8°C
• SMILES string: OC1COC(OC1)c2ccccc2
• InChI: 1S/C10H12O3/c11-9-6-12-10(13-7-9)8-4-2-1-3-5-8/h1-5,9-11H,6-7H2
• InChI key: BWKDAAFSXYPQOS-UHFFFAOYSA-N

Descripción

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.

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.

Información de seguridad

• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)