848302-38-5

Basic information

• Product Name: 2-Naphthalenol, 1-[(S)-[(2S,6R)-2-methyl-6-nonyl-1-piperidinyl]phenylmethyl]-
• CAS NO: 848302-38-5
• Molecular Formula: C32H43NO
• Molecular Weight: 457.7
• Mol File: 848302-38-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-Naphthalenol, 1-[(S)-[(2S,6R)-2-methyl-6-nonyl-1-piperidinyl]phenylmethyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Naphthalenol, 1-[(S)-[(2S,6R)-2-methyl-6-nonyl-1-piperidinyl]phenylmethyl]-(848302-38-5)
• EPA Substance Registry System: 2-Naphthalenol, 1-[(S)-[(2S,6R)-2-methyl-6-nonyl-1-piperidinyl]phenylmethyl]-(848302-38-5)

Safety Data

• Hazardous Substances Data: 848302-38-5(Hazardous Substances Data)

Upstream product

• 667870-42-0 (7aR,11R,13S)-11-(1H-benzotriazol-1-yl)-7a,8,10,11-tetrahydro-13-phenyl-9H,13H-naphtho[1,2-e]pyrido[2,1-b][1,3]oxazine 
• 848302-36-3 (7aR,11S,13S)-7a,8,10,11-tetrahydro-11-methyl-13-phenyl-9H,13H-naphtho[1,2-e]pyrido[2,1-b][1,3]oxazine 
• 39691-62-8 nonylmagnesium bromide 

Relevant articles and documents

Nonracemic betti base as a new chiral auxiliary: Application to total syntheses of enantiopure (2S,6R)-dihydropinidine and (2S,6R)-isosolenopsins

(Chemical Equation Presented) Total syntheses of enantiopure alkaloidal natural products (2S,6R)-dihydropinidine (as hydrochloride) and (2S,6R)-isosolenopsins (as hydrochlorides) were achieved in four steps and in 80-82% total yields by using a synthetic strategy of the formation-cleavage of 1,3-oxazinane. (S)-Betti base was proved to be an excellent chiral auxiliary and a novel Pd/C catalyzed N-debenzylation straightforward to amine hydrochloride was developed in the presence of CH2Cl2.