N-Boc-4-piperidineacetaldehyde

• Catalog No.: 680214
• CAS Number: 142374-19-4
• M. F.: C12H21NO3
• M. W.: 227.30004
• Purity: 97%

SYNONYMS

• Title: 4-(2-氧代乙基)哌啶-1-羧酸叔丁酯
• IUPAC name: tert-butyl 4-(2-oxoethyl)piperidine-1-carboxylate
• IUPAC Traditional name: tert-butyl 4-(2-oxoethyl)piperidine-1-carboxylate
• Synonyms: 1-(tert-butyloxycarbonyl)-piperidine-4-acetaldehyde; tert-Butyl 4-(formylmethyl)piperidine-1-carboxylate; 4-(2-Oxoethyl)piperidine-1-carboxylic acid, tert-butyl ester

DATABASE IDS

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

PROPERTIES

• Empirical Formula (Hill Notation): C12H21NO3
• Purity: 97%
• Flash Point: >110 °C
• Flash Point: >230 °F
• Melting Point: 38-42 °C
• GHS Signal Word: Warning
• GHS Hazard statements: H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
• GHS Precautionary statements: P261-P305 + P351 + P338
• Risk Statements: 36/37/38
• Safety Statements: 26
• German water hazard class: 3

DETAILS

Description (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

Description (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