182144-07-6

Basic information

• Product Name: 4-{1-[4-(4-methoxy-benzenesulfonyl)-phenyl]-vinyl}-[1,4']bipiperidinyl-1'-carboxylic acid tert-butyl ester
• Synonyms: 4-{1-[4-(4-methoxy-benzenesulfonyl)-phenyl]-vinyl}-[1,4']bipiperidinyl-1'-carboxylic acid tert-butyl ester
• CAS NO: 182144-07-6
• Molecular Weight: 540.724
• Mol File: 182144-07-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-{1-[4-(4-methoxy-benzenesulfonyl)-phenyl]-vinyl}-[1,4']bipiperidinyl-1'-carboxylic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-{1-[4-(4-methoxy-benzenesulfonyl)-phenyl]-vinyl}-[1,4']bipiperidinyl-1'-carboxylic acid tert-butyl ester(182144-07-6)
• EPA Substance Registry System: 4-{1-[4-(4-methoxy-benzenesulfonyl)-phenyl]-vinyl}-[1,4']bipiperidinyl-1'-carboxylic acid tert-butyl ester(182144-07-6)

Safety Data

• Hazardous Substances Data: 182144-07-6(Hazardous Substances Data)

Upstream product

• 315701-24-7 4-{1-[4-(4-methoxy-benzenesulfonyl)-phenyl]-vinyl}-piperidine-1-carboxylic acid tert-butyl ester 
• 315701-23-6 4-{1-[4-(4-methoxy-phenylsulfanyl)-phenyl]-vinyl}-piperidine-1-carboxylic acid tert-butyl ester 
• 182141-56-6 4-[4-(4-methoxy-phenylsulfanyl)-benzoyl]-piperidine-1-carboxylic acid tert-butyl ester 
• 160296-40-2 tert-butyl 1-[4-(4-fluorobenzoyl)piperidin-1-yl]carboxylate 
• 25519-78-2 4-(4-fluorobenzoyl)piperidine hydrochloride 
• 696-63-9 4-Methoxybenzenethiol 
• 79099-07-3 N-tert-butyloxycarbonylpiperidin-4-one 
• 315701-25-8 4-{1-[4-(4-methoxy-benzenesulfonyl)-phenyl]-vinyl}-piperidine 

Downstream Products

• 182144-25-8 4-{1-[4-(4-methoxy-benzenesulfonyl)-phenyl]-vinyl}-[1,4']bipiperidinyl 

Relevant articles and documents

Design and synthesis of piperidinyl piperidine analogues as potent and selective M2 muscarinic receptor antagonists

Identification of a number of highly potent M2 receptor antagonists with >100-fold selectivity against the M1 and M3 receptor subtypes is described. In the rat microdialysis assay, this series of compounds showed pronounced enhancement of brain acetylcholine release after oral administration. (C) 2000 Elsevier Science Ltd.