85518-76-9

Basic information

• Product Name: 3,5-dimethylphenylamine hydrochloride
• Synonyms: 3,5-dimethylphenylamine hydrochloride
• CAS NO: 85518-76-9
• Molecular Weight: 157.643
• Mol File: 85518-76-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3,5-dimethylphenylamine hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-dimethylphenylamine hydrochloride(85518-76-9)
• EPA Substance Registry System: 3,5-dimethylphenylamine hydrochloride(85518-76-9)

Safety Data

• Hazardous Substances Data: 85518-76-9(Hazardous Substances Data)

Upstream product

• 2050-45-5 N-acetyl-3,5-dimethylaniline 
• 925-90-6 ethylmagnesium bromide 
• 108-69-0 3,5-dimethylaminoaniline 

Downstream Products

• 87-85-4 Hexamethylbenzene 
• 2243-30-3 pentamethylaniline 
• 1639-31-2 3,4,5-trimethylaniline 
• 73351-87-8 5,7-dimethylbenzo[d]thiazol-2-amine 
• 1430208-73-3 N-(3,5-dimethylphenyl)-N'-[2-(trifluoromethyl)phenyl]guanidine 
• 1009646-66-5 C₂₇H₃₃N₅O 
• 103303-92-0 (3,5-Dimethyl-phenyl)-(1-morpholin-4-ylmethyl-5,6,7,8-tetrahydro-1H-pyrazolo[3,4-b]quinolin-4-yl)-amine 
• 103259-47-8 (3,5-Dimethyl-phenyl)-(1-piperidin-1-ylmethyl-5,6,7,8-tetrahydro-1H-pyrazolo[3,4-b]quinolin-4-yl)-amine 
• 103259-38-7 (3,5-Dimethyl-phenyl)-(5,6,7,8-tetrahydro-1H-pyrazolo[3,4-b]quinolin-4-yl)-amine 
• 100633-81-6 (3,5-Dimethyl-phenyl)-(5,6-dimethyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-amine 
• 120045-86-5 N⁶-(3,5-Dimethyl-phenyl)-9H-purine-2,6-diamine 

Relevant articles and documents

Reversible capture and release of aromatic amines by vicinal tricarbonyl compound

In this paper, we report reversible capture and release of aromatic amines by diphenylpropanetrione (DPPT). Addition of aromatic amines to the central carbonyl group occurred readily at ambient temperature to provide the aromatic amine adducts of DPPT (DPPT-aromatic amines), which has a hemiaminal structure. On the other hand, washing a solution of DPPT-aromatic amine with diluted hydrochloric acid (HCl) enabled successful recovery of DPPT to demonstrate the reversible nature of this system.

High-throughput approach for the identification of anilinium-based ionic liquids that are suitable for electropolymerisation

We report the synthesis of new protic ionic liquids (PILs) based on aniline derivatives and the use of high-throughput (HT) techniques to screen possible candidates. In this work, a simple HT method was applied to rapidly screen different aniline derivatives against different acids in order to identify possible combinations that produce PILs. This was followed by repeating the HT process with a Chemspeed robotic synthesis platform for more accurate results. One of the successful combinations were then chosen to be synthesised on a larger scale for further analysis. The new PILs are of interest to the fields of ionic liquids, energy storage and especially, conducting polymers as they serve as solvents, electrolytes and monomers at the same time for possible electropolymerisation (i.e. a self-contained polymer precursor).