(R)-2-苯氧甲基环氧乙烷

• 产品号: 29438
• CAS号: 71031-02-2
• 分子式: C9H10O2
• 分子量: 150.1745
• 纯 度: ≥97.0% (sum of enantiomers, GC)

产品别名

• 标题: (R)-2-Oxiranylanisole
• IUPAC标准名: (2R)-2-(phenoxymethyl)oxirane
• IUPAC传统名: (2R)-2-(phenoxymethyl)oxirane
• 别名: (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

产品登记号

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

产品性质

• Empirical Formula (Hill Notation): C9H10O2
• 纯度: ≥97.0% (sum of enantiomers, GC)
• 闪点: 71 °C
• 闪点: 159.8 °F
• GHS警示词: Danger
• GHS危险声明: H312-H315-H317-H318-H332-H335-H350
• 欧盟危险性物质标志: 有毒(Toxic) (T)
• 个人保护装置: Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
• GHS警示性声明: P201-P261-P280-P305 + P351 + P338-P308 + P313
• 危险公开号: 45-20/21-37/38-41-43-52/53-68
• 安全公开号: 53-26-36/37/39-45-61
• 德国WGK号: 3

产品详细信息

详细说明 (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

详细说明 (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