98977-55-0

Basic information

• Product Name: N-methyl-N-(3-phenylpropyl)-1-naphthalenemethanamine
• Synonyms: N-methyl-N-(3-phenylpropyl)-1-naphthalenemethanamine
• CAS NO: 98977-55-0
• Molecular Weight: 289.42
• Mol File: 98977-55-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N-methyl-N-(3-phenylpropyl)-1-naphthalenemethanamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-methyl-N-(3-phenylpropyl)-1-naphthalenemethanamine(98977-55-0)
• EPA Substance Registry System: N-methyl-N-(3-phenylpropyl)-1-naphthalenemethanamine(98977-55-0)

Safety Data

• Hazardous Substances Data: 98977-55-0(Hazardous Substances Data)

Upstream product

• 86-52-2 1-Chloromethylnaphthalene 
• 104-54-1 3-Phenylpropenol 
• 14489-75-9 N-methyl-1-naphthalenemethylamine 
• 98978-13-3 N-methyl-N-(naphthalen-1-ylmethyl)prop-2-en-1-amine 
• 65472-88-0 naftifine 
• 637-59-2 1-Bromo-3-phenylpropane 

Relevant articles and documents

PH-Mediated Selective Synthesis of N-Allylic Alkylation or N-Alkylation Amines with Allylic Alcohols via an Iridium Catalyst in Water

Amination of allylic alcohols is an effective approach in the facile synthesis of N-allylic alkylation or N-alkylation amines. Recently, a series of catalysts were devised to push forward this transformation. However, current synthetic methods are typical

Palladium-catalyzed regio- and stereoselective β-arylation of tertiary allylic amines: Identification of potent adenylyl cyclase inhibitors

Substituted allylic amines and their derivatives are key structural motifs of many drug molecules and natural products. A general, mild, and practical palladium-catalyzed β-arylation of tertiary allylic amines, one of the most challenging Heck arylation substrates, has been developed. The β-arylation products were obtained in excellent regio- and stereoselectivity. Moreover, novel and potent adenylyl cyclase inhibitors with the potential for treating neuropathic and inflammatory pain have been identified from the β-arylation products.