60000-09-1

Basic information

• Product Name: 1,2-DIPHENYLETHYLAMINE HYDROCHLORIDE
• Synonyms: Ethylamine, 1,2-diphenyl-, hydrochloride; alpha,beta-Diphenylaethylaminhydrochlorid [German]; Benzeneethanamine, .alpha.-phenyl-, hydrochloride; Benzeneethanamine, alpha-phenyl-, hydrochloride; Ethylamine, 1,2-diphenyl-, hydrochloride (8CI); 1,2-diphenylethanamine hydrochloride; Benzeneethanamine, alpha-phenyl-, hydrochloride (9CI); 1,2-diphenylethanamine; Phenethylamine, alpha-phenyl-, hydrochloride
• CAS NO: 60000-09-1
• Molecular Formula: C₁₄H₁₅N*ClH
• Molecular Weight: 233.76
• Mol File: 60000-09-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 311.1°Cat760mmHg
• Flash Point: 136.8°C
• Density: g/cm³
• CAS DataBase Reference: 1,2-DIPHENYLETHYLAMINE HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-DIPHENYLETHYLAMINE HYDROCHLORIDE(60000-09-1)
• EPA Substance Registry System: 1,2-DIPHENYLETHYLAMINE HYDROCHLORIDE(60000-09-1)

Safety Data

• Safety Statements: x and HCl. See also AMINES." target="_blank">Poison by subcutaneous, intravenous, and intraperitoneal routes. When heated to dec
• Hazardous Substances Data: 60000-09-1(Hazardous Substances Data)

Upstream product

• 451-40-1 phenyl benzyl ketone 
• 952-06-7 deoxybenzoin oxime 

Downstream Products

• 66730-28-7 N-(1,2-diphenylethyl)benzamide 
• 1106777-33-6 (R)-N-(1,2-diphenylethyl)benzamide 
• 1106777-47-2 (S)-N-(1,2-diphenylethyl)benzamide 
• 108478-16-6 3-Hydroxy-1,2-diphenyl-1-propanone 
• 5773-56-8 1,2-Diphenylethanol 

Relevant articles and documents

Regio- and stereoselective hydroamination of alkynes using an ammonia surrogate: Synthesis of N -Silylenamines as reactive synthons

An anti-Markovnikov selective hydroamination of alkynes with N-silylamines to afford N-silylenamines is reported. The reaction is catalyzed by a bis(amidate)bis(amido)Ti(IV) catalyst and is compatible with a variety of terminal and internal alkynes. Stoichiometric mechanistic studies were also performed. This method easily affords interesting N-silylenamine synthons in good to excellent yields and the easily removable silyl protecting group enables the catalytic synthesis of primary amines.

N6-SUBSTITUTED ADENOSINE DERIVATIVES, N6-SUBSTITUTED ADENINE DERIVATIVES AND USES THEREOF

The present invention provides N6-substituted adenosine derivatives and N6-substituted adenine derivatives, manufacturing methods thereof, a pharmaceutical composition comprising the said compounds above, and uses of of these compounds in manufacturing medicaments and health-care products for treating insomnia, convulsion, epilepsy, and Parkinson's diseases, and preventing and treating dementia.