5632-87-1

Basic information

• Product Name: N-benzoyl-L-norvaline
• CAS NO: 5632-87-1
• Molecular Weight: 221.256
• Mol File: 5632-87-1.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: N-benzoyl-L-norvaline(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzoyl-L-norvaline(5632-87-1)
• EPA Substance Registry System: N-benzoyl-L-norvaline(5632-87-1)

Safety Data

• Hazardous Substances Data: 5632-87-1(Hazardous Substances Data)

Upstream product

• 627-27-0 homoalylic alcohol 
• 201230-82-2 carbon monoxide 
• 55-21-0 benzamide 
• 4743-91-3 (R)-4-benzamino-penten-⁽¹⁾-oic acid-⁽⁵⁾ 
• 64-19-7 acetic acid 
• 7732-18-5 water 
• 98-88-4 benzoyl chloride 
• 5632-87-1 N-benzoylnorvaline 
• 760-78-1 2-aminopentanoic acid 
• 144447-82-5 D-norvaline ethyl ester 
• 2013-12-9 D-norvaline 
• 93-97-0 benzoic acid anhydride 
• 1896-62-4 (E)-benzalacetone 
• 6967-47-1 ethyl 2-cyanopentanoate 

Downstream Products

• 65-85-0 benzoic acid 
• 1242985-37-0 (R)-4-((R)-1-(4-chlorophenyl)-3-oxobutyl)-2-phenyl-4-propyloxazol-5(4H)-one 
• 1242985-40-5 (R)-4-((S)-1-(furan-2-yl)-3-oxobutyl)-2-phenyl-4-propyloxazol-5(4H)-one 
• 1242985-38-1 (R)-4-((R)-1-(2-chlorophenyl)-3-oxobutyl)-2-phenyl-4-propyloxazol-5(4H)-one 
• 1242985-39-2 (R)-4-((R)-1-(4-nitrophenyl)-3-oxobutyl)-2-phenyl-4-propyloxazol-5(4H)-one 
• 1242985-35-8 (R)-4-((R)-3-oxo-1-phenylbutyl)-2-phenyl-4-propyloxazol-5(4H)-one 
• 1242985-41-6 (R)-4-((R)-3-oxo-1,3-diphenylpropyl)-2-phenyl-4-propyloxazol-5(4H)-one 
• 1242985-36-9 (R)-4-((R)-1-(4-Methoxyphenyl)-3-oxobutyl)-2-phenyl-4-propyloxazol-5(4H)-one 
• 5632-87-1 N-benzoyl-D-norvaline 
• 5632-87-1 N-benzoyl-L-norvaline 

Relevant articles and documents

Nickel-Catalyzed Multicomponent Coupling: Synthesis of α-Chiral Ketones by Reductive Hydrocarbonylation of Alkenes

A nickel-catalyzed, multicomponent regio- and enantioselective coupling via sequential hydroformylation and carbonylation from readily available starting materials has been developed. This modular multicomponent hydrofunctionalization strategy enables the straightforward reductive hydrocarbonylation of a broad range of unactivated alkenes to produce a wide variety of unsymmetrical dialkyl ketones bearing a functionalized α-stereocenter, including enantioenriched chiral α-aryl ketones and α-amino ketones. It uses chiral bisoxazoline as a ligand, silane as a reductant, chloroformate as a safe CO source, and a racemic secondary benzyl chloride or an N-hydroxyphthalimide (NHP) ester of a protected α-amino acid as the alkylation reagent. The benign nature of this process renders this method suitable for late-stage functionalization of complex molecules.

Asymmetric palladium(II)-catalyzed cascade reaction giving quaternary amino succinimides by 1,4-addition and a nef-type reaction

Simple starting materials, high-value products: A dinuclear ferrocene-based PdII complex transforms mixtures of racemic N-benzoyl α-amino acids, nitroolefins, acetic anhydride, and manganese acetate into biologically interesting quaternary amin

Polyclonal antibodies: A cheap and efficient tool for screening of enantioselective catalysts

Enantioselective polyclonal antibodies have been produced and characterized to develop a high-throughput screening method for lipase activity fingerprinting, with a view to the enantioselective hydrolysis of azlactones.