313266-11-4

Basic information

• Product Name: N¹,N⁴-dibenzyl-2,3-dihydroxysuccinamide
• Synonyms: N¹,N⁴-dibenzyl-2,3-dihydroxysuccinamide
• CAS NO: 313266-11-4
• Molecular Weight: 328.368
• Mol File: 313266-11-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N¹,N⁴-dibenzyl-2,3-dihydroxysuccinamide(CAS DataBase Reference)
• NIST Chemistry Reference: N¹,N⁴-dibenzyl-2,3-dihydroxysuccinamide(313266-11-4)
• EPA Substance Registry System: N¹,N⁴-dibenzyl-2,3-dihydroxysuccinamide(313266-11-4)

Safety Data

• Hazardous Substances Data: 313266-11-4(Hazardous Substances Data)

Upstream product

• 408332-88-7 Diethyl tartrate 
• 100-46-9 benzylamine 
• 87-69-4 tartaric acid 

Downstream Products

• 1450908-81-2 (R)-N-benzyl-1-(4-methoxyphenyl)-6-methyl-4-phenyl-1,4-dihydropyridazine-3-carboxamide 
• 1450909-02-0 (E)-N-benzyl-2-(2-(4-methoxyphenyl)hydrazono)acetamide 
• 108321-43-3 N,N'-dibenzyl-(S,S)-tartaric acid diamide 
• 88393-56-0 (2R,3R)-N¹,N⁴-dibenzyl-2,3-dihydroxysuccinamide 
• 32331-52-5 N-benzyl glyoxylic amide 

Relevant articles and documents

Catalytic asymmetric construction of chiral hydropyridazines via conjugate addition of N-monosubstituted hydrazones to enones

The first example of a highly enantioselective and scalable formal diaza-ene reaction between N-monosubstituted hydrazones and enones catalyzed by a simple chiral primary-second diamine salt has been developed. The catalytic process provides a highly prac

Amino amides, peptides and peptidomimetics

Synthetic methods and compounds involving amino amides, peptides and peptidomimetics. Amino amide derivatives are prepared via the one-step three-component reaction of a glyoxamide, an amine, and an organoboron derivative. Conversion of the product to another glyoxamide intermediate allows the iterative use of this chemistry for the synthesis of peptides and peptidomimetics.