210106-84-6

Basic information

• Product Name: N¹-benzylsuccinamide
• Synonyms: N¹-benzylsuccinamide
• CAS NO: 210106-84-6
• Molecular Weight: 206.244
• Mol File: 210106-84-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N¹-benzylsuccinamide(CAS DataBase Reference)
• NIST Chemistry Reference: N¹-benzylsuccinamide(210106-84-6)
• EPA Substance Registry System: N¹-benzylsuccinamide(210106-84-6)

Safety Data

• Hazardous Substances Data: 210106-84-6(Hazardous Substances Data)

Upstream product

• 100-44-7 benzyl chloride 
• 108-30-5 succinic acid anhydride 
• 100-46-9 benzylamine 
• 638-32-4 succinamic acid 
• 2142-06-5 1-(phenylmethyl)-2,5-pyrrolidinedione 

Downstream Products

• 310873-78-0 (3-benzylcarbamoyl-propionylamino)-acetic acid tert-butyl ester 
• 310873-79-1 N-(benzylaminocarbonylpropyl)glycine 

Relevant articles and documents

The mechanism of cleavage under basic conditions of succinyl-anchored oligonucleotides

Studies with a model compound provide direct evidence that cleavage of succinyl-anchored oligonucleotides takes place by intramolecular nucleophilic attack of the conjugate base of the succinamide at the ester carbonyl group. An N-substituted succinamide is exclusively formed with piperidine, DBU and TBAF, but when ammonia is used this general mechanism seems to coexist with ammonolysis of the succinate ester. Cleavage with TBAF is extremely fast.

Novel α-amino acid-based hydroxamic acid ligands for vanadium-catalyzed asymmetric epoxidation of allylic alcohols [2]

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