386702-67-6

Basic information

• Product Name: (R)-3-(2-bromo-phenoxy)-propane-1,2-diol
• Synonyms: (R)-3-(2-bromo-phenoxy)-propane-1,2-diol
• CAS NO: 386702-67-6
• Molecular Weight: 247.089
• Mol File: 386702-67-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (R)-3-(2-bromo-phenoxy)-propane-1,2-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-3-(2-bromo-phenoxy)-propane-1,2-diol(386702-67-6)
• EPA Substance Registry System: (R)-3-(2-bromo-phenoxy)-propane-1,2-diol(386702-67-6)

Safety Data

• Hazardous Substances Data: 386702-67-6(Hazardous Substances Data)

Upstream product

• 63834-58-2 rac-3-(2-bromophenoxy)propane-1,2-diol 
• 95-56-7 2-hydroxybromobenzene 
• 65031-96-1 (S)-glycidyl butyrate 
• 57044-25-4 (R)-oxiranemethanol 

Downstream Products

• 62501-72-8 (R)-2-hydroxymethyl-1,4-benzodioxane 

Relevant articles and documents

Absolute configuration and crystal packing chirality for three conglomerate-forming ortho-halogen substituted phenyl glycerol ethers

Three conglomerate-forming ortho-Hal (Hal = Cl, Br, I) substituted phenyl glycerol ethers 1-3 were investigated by single-crystal X-ray analysis, and the absolute configuration for all substances was established. The molecular structures and crystal packi

Crystallization of chiral compounds 3. 3-Phenoxypropane-1,2-diol and 3-(2-halophenoxy)propane-1,2-diols

Specific features of melting of crystalline samples of 3-(2-R-phenoxy) propane-1,2-diols with different enantiomeric compositions were studied by differential scanning calorimetry. The melting points and enthalpies of melting for the racemate and individual stereoisomers were determined. Binary phase diagrams were constructed. The entropy of mixing of individual enantiomers in the liquid phase and the free energy of formation of the racemic compound were calculated. The thermochemical data indicate that the racemates are formed upon the crystallization of phenoxy-and 2-fluorophenoxy-containing compounds, while crystallization of the chloro-, bromo-, and iodo-substituted analogs would form racemic conglomerates.