4-(2-氧代乙基)哌啶-1-羧酸叔丁酯

• 产品号: 680214
• CAS号: 142374-19-4
• 分子式: C12H21NO3
• 分子量: 227.30004
• 纯 度: 97%

产品别名

• 标题: N-Boc-4-piperidineacetaldehyde
• IUPAC标准名: tert-butyl 4-(2-oxoethyl)piperidine-1-carboxylate
• IUPAC传统名: tert-butyl 4-(2-oxoethyl)piperidine-1-carboxylate
• 别名: 1-(tert-butyloxycarbonyl)-piperidine-4-acetaldehyde; tert-Butyl 4-(formylmethyl)piperidine-1-carboxylate; 4-(2-Oxoethyl)piperidine-1-carboxylic acid, tert-butyl ester

产品登记号

• PubChem SID: 24885547
• MDL号: MFCD03425258
• CAS号: 142374-19-4

产品性质

• Empirical Formula (Hill Notation): C12H21NO3
• 纯度: 97%
• 闪点: >110 °C
• 闪点: >230 °F
• 熔点: 38-42 °C
• GHS警示词: Warning
• GHS危险声明: H315-H319-H335
• 欧盟危险性物质标志: 刺激性(Irritant) (Xi)
• 个人保护装置: dust mask type N95 (US), Eyeshields, Gloves
• GHS警示性声明: P261-P305 + P351 + P338
• 危险公开号: 36/37/38
• 安全公开号: 26
• 德国WGK号: 3

产品详细信息

详细说明 (English)

Application
Building block employed in a synthesis of (S)-quinuclidine-2-carboxylic acid.7 Substrate used in an enanioselective organo-catalytic α-vinylation reaction.8
Reactant for synthesis of:
• Pim-1 inhibitors1
• Selective GPR119 agonists for type II diabetes2,3Reactant for:
• α-arylation of aldehydes4
• Enantioselective α-benzylation of aldehydes via photoredox organocatalysis5
• Enantioselective α-triflouromethylation of aldehydes6
Packaging
1 g in glass bottle

详细说明 (简体中文)

Application
用于合成 (S)-奎宁环-2-羧酸的结构单元。7用于不对称有机催化 α-乙烯化反应的底物。8
Reactant for synthesis of:
• Pim-1 inhibitors1
• Selective GPR119 agonists for type II diabetes2,3Reactant for:
• α-arylation of aldehydes4
• Enantioselective α-benzylation of aldehydes via photoredox organocatalysis5
• Enantioselective α-triflouromethylation of aldehydes6
包装
1 g in glass bottle