880169-79-9

Basic information

• Product Name: 1-Piperazinecarboxylic acid, 6-[3-[[bis[[(1,1-dimethylethoxy)carbonyl]amino]methylene]amino]propyl]- 4-[(3,4-difluorophenyl)methyl]-2-(2-naphthalenylmethyl)-3-oxo-, 1,1-dimethylethyl ester, (2R,6R)-
• CAS NO: 880169-79-9
• Molecular Formula: C41H53F2N5O7
• Molecular Weight: 765.898
• Mol File: 880169-79-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-Piperazinecarboxylic acid, 6-[3-[[bis[[(1,1-dimethylethoxy)carbonyl]amino]methylene]amino]propyl]- 4-[(3,4-difluorophenyl)methyl]-2-(2-naphthalenylmethyl)-3-oxo-, 1,1-dimethylethyl ester, (2R,6R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Piperazinecarboxylic acid, 6-[3-[[bis[[(1,1-dimethylethoxy)carbonyl]amino]methylene]amino]propyl]- 4-[(3,4-difluorophenyl)methyl]-2-(2-naphthalenylmethyl)-3-oxo-, 1,1-dimethylethyl ester, (2R,6R)-(880169-79-9)
• EPA Substance Registry System: 1-Piperazinecarboxylic acid, 6-[3-[[bis[[(1,1-dimethylethoxy)carbonyl]amino]methylene]amino]propyl]- 4-[(3,4-difluorophenyl)methyl]-2-(2-naphthalenylmethyl)-3-oxo-, 1,1-dimethylethyl ester, (2R,6R)-(880169-79-9)

Safety Data

• Hazardous Substances Data: 880169-79-9(Hazardous Substances Data)

Upstream product

• 880169-78-8 4-(3,4-difluorobenzyl)-6-(3-hydroxy-propyl)-2-naphthalen-2-ylmethyl-3-oxo-piperazine-1-carboxylic acid tert-butyl ester 
• 332882-82-3 1,3-bis(t-butoxycarbonyl)guanidine 
• 170899-08-8 N-(tert-butoxycarbonyl)-D-allylglycine 
• 72235-53-1 3,4-difluorobenzylamine 
• 880169-77-7 2-allyl-4-(3,4-difluorobenzyl)-2-naphthalen-2-ylmethyl-3-oxo-piperazine-1-carboxylic acid tert-butyl ester 
• 880169-76-6 2-allyl-4-(3,4-difluorobenzyl)-5-oxo-piperazine-1-carboxylic acid tert-butyl ester 
• 880169-75-5 {1-[(3,4-difluorobenzylamino)-methyl]-but-3-enyl}-carbamic acid tert-butyl ester 

Relevant articles and documents

Ketopiperazines: Conformationally constrained peptidomimetic of arginine amides

We have synthesized guanidine-containing ketopiperazines designed to be conformational mimics of peptidomimetic arginine amides. D-Allylglycine was converted by an efficient approach to give enantiopure ketopiperazines in which the trans stereochemistry o