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29438 Sigma-Aldrich

(R)-2-Oxiranylanisole

≥97.0% (sum of enantiomers, GC)

Synonym: (R)-α-(2-Oxiranyl)anisole, (R)-Glycidyl phenyl ether, (R)-Phenoxymethyloxirane

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Properties

Related Categories Asymmetric Synthesis, Chemical Synthesis, Chiral Building Blocks, Epoxides, Organic Building Blocks More...
InChI Key   FQYUMYWMJTYZTK-VIFPVBQESA-N
assay   ≥97.0% (sum of enantiomers, GC)

Description

Application

Reactant involved in the synthesis of:
• Neuroprotective small molecules
• Piperidinol analogs for studies of anti-tuberculosis activity
• 2-Substituted 3,4-dihydro-2H-1,4-benzoxazines via cyclization of hydroxyl sulfonamides
• Bicyclic azetidines via ring opening, esterification, chlorination and intramolecular alkylation
• Bromoalkanes via ring opening and addition across C-O bonds

Involved in biological studies as a substrate for Bacillus-produced enantioselective eposide hydrolase

Packaging

1 g in glass bottle

Safety & Documentation

Safety Information

Symbol 
Signal word 
Danger
RIDADR 
NA 1993 / PGIII
WGK Germany 
3
Flash Point(F) 
159.8 °F
Flash Point(C) 
71 °C

Documents

Certificate of Analysis

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Protocols & Articles
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