(R)-2-Oxiranylanisole

• Catalog No.: 29438
• CAS Number: 71031-02-2
• M. F.: C9H10O2
• M. W.: 150.1745
• Purity: ≥97.0% (sum of enantiomers, GC)

SYNONYMS

• Title: (R)-2-苯氧甲基环氧乙烷
• IUPAC name: (2R)-2-(phenoxymethyl)oxirane
• IUPAC Traditional name: (2R)-2-(phenoxymethyl)oxirane
• Synonyms: (R)-α-(2-环氧乙基)苯甲醚; (R)-Phenoxymethyloxirane; (R)-缩水甘油基苯基醚; (R)-α-(2-Oxiranyl)anisole; (R)-Glycidyl phenyl ether

DATABASE IDS

• CAS Number: 71031-02-2
• MDL Number: MFCD06659025
• PubChem SID: 24857711

PROPERTIES

• Empirical Formula (Hill Notation): C9H10O2
• Purity: ≥97.0% (sum of enantiomers, GC)
• Flash Point: 71 °C
• Flash Point: 159.8 °F
• GHS Signal Word: Danger
• GHS Hazard statements: H312-H315-H317-H318-H332-H335-H350
• European Hazard Symbols: Toxic (T)
• Personal Protective Equipment: Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
• GHS Precautionary statements: P201-P261-P280-P305 + P351 + P338-P308 + P313
• Risk Statements: 45-20/21-37/38-41-43-52/53-68
• Safety Statements: 53-26-36/37/39-45-61
• German water hazard class: 3

DETAILS

Description (English)

Packaging
1 g in glass bottle
Application
Reactant involved in the synthesis of:
• Neuroprotective small molecules1
• Piperidinol analogs for studies of anti-tuberculosis activity2
• 2-Substituted 3,4-dihydro-2H-1,4-benzoxazines via cyclization of hydroxyl sulfonamides3
• Bicyclic azetidines via ring opening, esterification, chlorination and intramolecular alkylation4
• Bromoalkanes via ring opening and addition across C-O bonds5Involved in biological studies as a substrate for Bacillus-produced enantioselective eposide hydrolase6

Description (简体中文)

包装
1 g in glass bottle
Application
Reactant involved in the synthesis of:
• Neuroprotective small molecules1
• Piperidinol analogs for studies of anti-tuberculosis activity2
• 2-Substituted 3,4-dihydro-2H-1,4-benzoxazines via cyclization of hydroxyl sulfonamides3
• Bicyclic azetidines via ring opening, esterification, chlorination and intramolecular alkylation4
• Bromoalkanes via ring opening and addition across C-O bonds5Involved in biological studies as a substrate for Bacillus-produced enantioselective eposide hydrolase6