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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

  • CAS Number 71031-02-2

  • Empirical Formula (Hill Notation) C9H10O2

  • Molecular Weight 150.17

  •  MDL number MFCD06659025

  •  PubChem Substance ID 57648370

  •  NACRES NA.22

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Properties

Related Categories Asymmetric Synthesis, Chemical Synthesis, Chiral Building Blocks, Epoxides, Organic Building Blocks More...
assay   ≥97.0% (sum of enantiomers, GC)
storage temp.   room temp
SMILES string   C1O[C@H]1COc2ccccc2
InChI   1S/C9H10O2/c1-2-4-8(5-3-1)10-6-9-7-11-9/h1-5,9H,6-7H2/t9-/m0/s1
InChI key   FQYUMYWMJTYZTK-VIFPVBQESA-N

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
Target organs 
Respiratory system
RIDADR 
NA 1993 / PGIII
WGK Germany 
WGK 3
Flash Point(F) 
159.8 °F - closed cup
Flash Point(C) 
71 °C - closed cup

Documents

Certificate of Analysis (COA)

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Protocols & Articles
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