42164-56-7

Basic information

• Product Name: N,N-dibenzylpropane-1,2-diamine
• Synonyms: N,N-dibenzylpropane-1,2-diamine
• CAS NO: 42164-56-7
• Molecular Formula: C₁₇H₂₂N₂
• Molecular Weight: 254.37
• Mol File: 42164-56-7.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 382.3 °C at 760 mmHg
• Flash Point: 223 °C
• Appearance: /
• Density: 1.015 g/cm³
• PKA: 8.94±0.19(Predicted)
• CAS DataBase Reference: N,N-dibenzylpropane-1,2-diamine(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-dibenzylpropane-1,2-diamine(42164-56-7)
• EPA Substance Registry System: N,N-dibenzylpropane-1,2-diamine(42164-56-7)

Safety Data

• Hazardous Substances Data: 42164-56-7(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 78-90-0 1,2-diaminopropan 
• 57-55-6 propylene glycol 
• 103-49-1 dibenzylamine 
• 133695-14-4 N,N'-dibenzylidenepropane-1,2-diamine 
• 100-46-9 benzylamine 
• 42164-52-3 1,3-dibenzyl-4-methyl-2-phenyl-imidazolidine 

Downstream Products

• 1354623-70-3 5,8-dibenzyl-7-methyl-5,8-diazaspiro[2.6]nonane 
• 75825-40-0 N,N'-dibenzyl-5-methyloctahydro-1,4,7-oxadiazonine 

Relevant articles and documents

METHOD FOR SYNTHESIZING AMINES

The invention relates to a process for preparing certain amines, wherein, in a first step, a corresponding amino alcohol is reacted with a suitable carbonyl compound and then, in a second step, the intermediate obtained in the first step is reacted with a suitable amine component to form the desired amine.

NOVEL HOMOPIPERAZINE DERIVATIVES AS PROTEIN TYROSINE KINASE INHIBITORS AND PHARMACEUTICAL USE THEREOF

The invention relates to compounds of general formula (I) wherein R1,R2, R3, R4, m and n are defined as defined herein, and pharmaceutically acceptable salts, hydrates, or solvates thereof, for use -alone or in

Synthesis and antitubercular activity of ferrocenyl diaminoalcohols and diamines

A total of 21 ferrocenyl and benzyl diaminoalcohols and diamines were synthesized and evaluated against Mycobacterium tuberculosis H37Rv. Interestingly, ferrocenyl diamines exhibit better activities than ferrocenyl diaminoalcohols.