6297-57-0

Basic information

• Product Name: N-(benzylsulfonyl)leucine
• Synonyms: 2-[(benzylsulfonyl)amino]-4-methylpentanoic acid
• CAS NO: 6297-57-0
• Molecular Formula: C₁₃H₁₉NO₄S
• Molecular Weight: 285.3593
• Mol File: 6297-57-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 464.1°C at 760 mmHg
• Flash Point: 234.5°C
• Density: 1.24g/cm³
• Vapor Pressure: 2.05E-09mmHg at 25°C
• Refractive Index: 1.549
• CAS DataBase Reference: N-(benzylsulfonyl)leucine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(benzylsulfonyl)leucine(6297-57-0)
• EPA Substance Registry System: N-(benzylsulfonyl)leucine(6297-57-0)

Safety Data

• Hazardous Substances Data: 6297-57-0(Hazardous Substances Data)

Upstream product

• 138535-51-0 N-(phenylmethanesulfonyl)-L-leucine methyl ester 
• 7517-19-3 methyl (L)-leucinate hydrochloride 
• 1939-99-7 benzenesulfonyl chloride 
• 1738-77-8 L-leucine benzyl ester p-toluenesulfonate 
• 61-90-5 L-leucine 
• 102322-09-8 N-phenylmethanesulfonyl-L-leucine-(N'-phenyl-hydrazide) 

Downstream Products

• 131733-31-8 N-phenylmethanesulfonyl-L-leucyl chloride 
• 663923-87-3 N-(phenylmethanesulfonyl)-L-leucyl-L-proline methyl ester 
• 663923-88-4 N-(phenylmethanesulfonyl)-L-leucyl-L-proline 
• 663923-89-5 1-[N²,N³-bis(tert-butyloxycarbonyl)guanidino]-4-(N-phenylmethanesulfonyl-L-leucyl-L-prolyl-amino)butane 
• 1374962-78-3 N-benzylsulfonyl-D,L-leucyl-L-proline-[(4-cyanophenyl)methyl]amide 
• 3253-28-9 N-(N-phenylmethanesulfonyl-L-leucyl)-L-leucine ethyl ester 
• 7474-68-2 N-(N-phenylmethanesulfonyl-L-leucyl)-L-leucine 
• 3303-31-9 L-leucyl-L-leucine 
• 102322-09-8 N-phenylmethanesulfonyl-L-leucine-(N'-phenyl-hydrazide) 

Relevant articles and documents

MODULATORS OF SESTRIN-GATOR2 INTERACTION AND USES THEREOF

The present invention provides compounds, compositions thereof, and methods of using the same.

PROLINAMIADE DERIVATIVES AS THROMBIN INHIBITOR, PREPRARATION METHOD AND APPLICATION THEREOF

Provided are a compound of formula (I), pharmaceutically acceptable salts thereof, preparation methods and applications thereof for inhibiting thrombin, and applications in the treatment and prevention of thrombin-mediated and thrombin-related diseases.