89728-15-4

Basic information

• Product Name: 2,3-Diamino-4,6-dimethyl-5-bromopyridine
• Synonyms: 2,3-Diamino-4,6-dimethyl-5-bromopyridine;5-BroMo-4,6-diMethylpyridine-2,3-diaMine
• CAS NO: 89728-15-4
• Molecular Formula: C₇H₁₀BrN₃
• Molecular Weight: 216.0784
• Mol File: 89728-15-4.mol
• Article Data: 4

Chemical Properties

• Melting Point: 239℃ (ethanol )
• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: 2,3-Diamino-4,6-dimethyl-5-bromopyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-Diamino-4,6-dimethyl-5-bromopyridine(89728-15-4)
• EPA Substance Registry System: 2,3-Diamino-4,6-dimethyl-5-bromopyridine(89728-15-4)

Safety Data

• Hazardous Substances Data: 89728-15-4(Hazardous Substances Data)

Usage

General Description

2,3-Diamino-4,6-dimethyl-5-bromopyridine is a chemical compound with the molecular formula C7H10BrN3. It is a derivative of pyridine and contains two amino groups, two methyl groups, and a bromine atom. 2,3-Diamino-4,6-dimethyl-5-bromopyridine is commonly used as a building block in the synthesis of pharmaceuticals, agrochemicals, and organic materials. It is an important intermediate in the production of various biologically active compounds and is used in the research and development of new drugs. Additionally, it has potential applications in the field of materials science and nanotechnology due to its unique chemical properties. Overall, 2,3-Diamino-4,6-dimethyl-5-bromopyridine is a versatile chemical with applications in various industries.

InChI:InChI=1S/C7H10BrN3/c1-3-5(8)4(2)11-7(10)6(3)9/h9H2,1-2H3,(H2,10,11)

Upstream product

• 89791-76-4 2-amino-3-nitro-4,6-dimethyl-5-bromo-pyridine 
• 98950-02-8 (2-amino-5-bromo-4,6-dimethyl-[3]pyridyl)-carbamic acid methyl ester 
• 5407-87-4 2-Amino-4,6-dimethylpyridine 
• 89856-44-0 2-amino-5-bromo-4,6-dimethylpyridine 

Downstream Products

• 92336-10-2 6-bromo-5,7-dimethyl-1⁽³⁾H-imidazo[4,5-b]pyridine 
• 121655-34-3 6-bromo-5,7-dimethyl-1H-[1,2,3]triazolo[4,5-b]pyridine 
• 116599-55-4 5,7-dimethyl-1(3)H-imidazo[4,5-b]pyridine 
• 114163-51-8 5,7-dimethyl-1H-[1,2,3]triazolo[4,5-b]pyridine 

Relevant articles and documents

First demonstration of positive allosteric-like modulation at the human wild type translocator protein (TSPO)

We show that changing the number and position of nitrogen atoms in the heteroatomic core of a pyrazolopyrimidine acetamide is sufficient to induce complex binding to wild type human TSPO. Only compounds with this complex binding profile lacked intrinsic effect on glioblastoma proliferation but positively modulated the antiproliferative effects of a synthetic TSPO ligand. To the best of our knowledge this is the first demonstration of allosteric-like interaction at the wild type human TSPO.

PYRIDYL IMIDAZOLE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF

Substituted pyridyl imidazole derivatives of formula (I) inhibit effectively the action of angiotensin II and have a superior anti-hypertensive activity. STR1