98053-41-9

Basic information

• Product Name: N-(1,7,7-trimethylnorbornyl)benzamide
• CAS NO: 98053-41-9
• Molecular Weight: 257.376
• Mol File: 98053-41-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N-(1,7,7-trimethylnorbornyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(1,7,7-trimethylnorbornyl)benzamide(98053-41-9)
• EPA Substance Registry System: N-(1,7,7-trimethylnorbornyl)benzamide(98053-41-9)

Safety Data

• Hazardous Substances Data: 98053-41-9(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 1159913-50-4 (1R)-isobornylamine hydrochloride 
• 5794-04-7 camphene 
• 100-47-0 benzonitrile 
• 24393-70-2 isoborneol 
• 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 

Downstream Products

• 101892-69-7 2-endo-benzoylamino, N-methyl, bornane 
• 101892-69-7 2-exo-benzoylamino, N-methyl, bornane 
• 111013-46-8 5-exo-acetoxy, 2-exo-benzoylamino, bornane 
• 111013-48-0 2-exo benzoylamino, 5-oxo, bornane 
• 102992-43-8 2-exo-benzoylamino, 5-exo-hydroxy, bornane 
• 102992-43-8 2-exo-benzoylamino, 5-exo-hydroxy, bornane 

Relevant articles and documents

A direct and stereoretentive synthesis of amides from cyclic alcohols

Chlorosulfites prepared in situ using thionyl chloride react with nitrile complexes of titanium(IV) fluoride to give a one-pot conversion of alcohols into amides. For the first time, amides are obtained from cyclic alcohols with stereoretention. Critical to the design of these new TiIV reactions has been the use of little-explored TiIV nitrile complexes that are thought to chelate chlorosulfites in the transition state tocreate a carbocation that is rapidly captured by the nitrile nucleophile through a front-side attack mechanism.

MICROBIAL TRANSFORMATIONS. PART 7 (1) BIOHYDROXYLATION OF BORNYLAMIDE DERIVATIVES BY THE FUNGUS BEAUVERIA SULFURESCENS

The biohydroxylation of various amide derivatives of norbornane and of camphane have been studied, in order to explore the possible influence of this amide group configuration and substitution upon the regio, the stereo and the enantioselectivity of the p