105615-60-9

Basic information

• Product Name: 2-endo-benzoylamino, bornane
• Synonyms: 2-endo-benzoylamino, bornane
• CAS NO: 105615-60-9
• Molecular Weight: 257.376
• Mol File: 105615-60-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-endo-benzoylamino, bornane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-endo-benzoylamino, bornane(105615-60-9)
• EPA Substance Registry System: 2-endo-benzoylamino, bornane(105615-60-9)

Safety Data

• Hazardous Substances Data: 105615-60-9(Hazardous Substances Data)

Upstream product

• 5794-04-7 camphene 
• 100-47-0 benzonitrile 
• 24393-70-2 isoborneol 
• 98-88-4 benzoyl chloride 
• 464-42-6 (1S,2R,4S)-1,7,7-Trimethyl-bicyclo[2.2.1]hept-2-ylamine 
• 464-43-7 borneol 
• 72257-25-1 isocamphanol 
• 1159913-50-4 (1R)-isobornylamine hydrochloride 
• 464-43-7 d-borneol 
• 4481-88-3 bornylamine 
• 32511-34-5 (R)-Bornylamine 

Downstream Products

• 111013-46-8 5-exo-acetoxy, 2-exo-benzoylamino, bornane 
• 111013-48-0 2-exo benzoylamino, 5-oxo, bornane 
• 101892-69-7 2-exo-benzoylamino, N-methyl, bornane 
• 102992-43-8 2-exo-benzoylamino, 5-exo-hydroxy, bornane 
• 101892-69-7 2-endo-benzoylamino, N-methyl, bornane 
• 102992-43-8 2-exo-benzoylamino, 5-exo-hydroxy, bornane 
• 111013-49-1 Acetic acid (1R,2S,4R,7R)-2-benzoylamino-1,7-dimethyl-bicyclo[2.2.1]hept-7-ylmethyl ester 
• 111137-89-4 Acetic acid (1R,2S,4R,7S)-2-benzoylamino-1,7-dimethyl-bicyclo[2.2.1]hept-7-ylmethyl ester 
• 111058-95-8 Acetic acid (1R,2R,4R,5S)-5-benzoylamino-4,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester 

Relevant articles and documents

Magnetic CoFe2O4 nanoparticle immobilized N-propyl diethylenetriamine sulfamic acid as an efficient and recyclable catalyst for the synthesis of amides via the Ritter reaction

A magnetic CoFe2O4 nanoparticle immobilized diamine-N-sulfamic acid (CoFe2O4@SiO2-DASA) was synthesized and used as efficient heterogeneous catalyst for the synthesis of amides via the Ritter reaction under solvent-free conditions. The magnetic nanocatalyst could be readily recovered by applying an external magnet and recycled several times without considerable loss of its catalytic activity.

Synthesis of N-substituted amides by the Ritter reaction with heteropoly acids as catalysts

Reactions of a number of nitriles with camphene in the presence of the heteropoly acids H3PW12O40, H 7PMo12O42, and H4SiW 12O40 as catalysts were studied. I

RITTER REACTION OF 5,5,6-TRIMETHYLBICYCLOHEPTAN-2-EXO-OL WITH ACETO- AND BENZONITRILE

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