151095-68-0

Basic information

• Product Name: N-Benzoyl-2-hydroxy-hexahydrobenzylamin
• Synonyms: N-Benzoyl-2-hydroxy-hexahydrobenzylamin
• CAS NO: 151095-68-0
• Molecular Weight: 233.31
• Mol File: 151095-68-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-Benzoyl-2-hydroxy-hexahydrobenzylamin(CAS DataBase Reference)
• NIST Chemistry Reference: N-Benzoyl-2-hydroxy-hexahydrobenzylamin(151095-68-0)
• EPA Substance Registry System: N-Benzoyl-2-hydroxy-hexahydrobenzylamin(151095-68-0)

Safety Data

• Hazardous Substances Data: 151095-68-0(Hazardous Substances Data)

Upstream product

• 63301-31-5 trans-2-cyanocyclohexanol 
• 98-88-4 benzoyl chloride 
• 109087-14-1 trans-2-(aminomethyl)cyclohexanol 
• 110-83-8 cyclohexene 
• 6282-02-6 N-(hydroxymethyl)benzamide 
• 13727-29-2 cis-5,6-cyclohexylene-5,6-dihydro-2-phenyl-4H-1,3-oxazine 
• 13727-29-2 1-phenyl-5,6-dihydro-4H-1,3-oxazine 
• 55-21-0 benzamide 

Downstream Products

• 126675-20-5 (1R,2R)-2-(Isopropylamino-methyl)-cyclohexanol 
• 126675-19-2 (1R,2R)-2-Cyclohexylaminomethyl-cyclohexanol 
• 94819-68-8 cis-5,6-tetramethylene-5,6-dihydro-2-phenyl-4H-1,3-thiazine 
• 94819-68-8 trans-5,6-tetramethylene-5,6-dihydro-2-phenyl-<4H>-1,3-thiazine 
• 97942-10-4 cis-5,6-cyclohexylene-5,6-dihydro-2-phenyl-4H-1,3-thiazine perchlorate salt 
• 88413-44-9 Cyclohexanespiro-5'-(2'-phenylthiazoline) 
• 77612-17-0 cis-N-benzyl-2-aminomethyl-1-cyclohexanol 

Relevant articles and documents

Synthesis and some transformations of substituted 5,6-dihydro-4H-1,3-oxazines

Substituted 5,6-dihydro-4H-1,3-oxazines are prepared by the acid-catalyzed amidoalkylation of the terminal olefins. 5,6-Dihydro-4H-oxazines undergo further transformations involving the hetero-ring and/or the substituent leading to alkyl amino-substituted

STEREOCHEMICAL STUDIES, 80. CYCLIC AMINOALCOHOLS AND RELATED COMPOUNDS, 26. PREPARATION OF CIS-2-(ALKYLAMINOMETHYL)- AND (ARALKYLAMINOMETHYL)-1-CYCLANOLS FROM OLEFINS VIA THE 5,6-DIHYDRO-4H-1,3-OXAZINE DERIVATIVES

Cycloalkenes were allowed to react with N-(hydroxymethyl)alkyl- or -arylamides in the presence of concentrated sulfuric acid in glacial acetic acid, using the method suggested by Schmidt.In the majority of cases, the reaction yielded the corresponding cis