1073-21-8

Basic information

• Product Name: 3-Amino-2,4-dimethylpyridine
• Synonyms: 3-AMINO-2,4-DIMETHYLPYRIDINE;3-Amino-2,4-dimethylpyridine 97%;2,4-dimethylpyridin-3-amine;2,4-diMethyl-3-PyridinaMine;PyriMido[1,2-b]pyridazin-2-one;2,4-Dimethylpyridin-3-amine, 3-Amino-2,4-lutidine;3-Amino-2,4-dimethylpyridine97%
• CAS NO: 1073-21-8
• Molecular Formula: C₇H₁₀N₂
• Molecular Weight: 122.17
• Product Categories: Heterocyclic Compound;Amines;Pyridines
• Mol File: 1073-21-8.mol
• Article Data: 6

Chemical Properties

• Melting Point: 53 °C
• Boiling Point: 255.708 °C at 760 mmHg
• Flash Point: 132.153 °C
• Appearance: Pale brown/Crystalline Powder
• Density: 1.04 g/cm³
• Vapor Pressure: 0.016mmHg at 25°C
• Refractive Index: 1.564
• Storage Temp.: 2-8°C
• PKA: 7.54±0.18(Predicted)
• CAS DataBase Reference: 3-Amino-2,4-dimethylpyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Amino-2,4-dimethylpyridine(1073-21-8)
• EPA Substance Registry System: 3-Amino-2,4-dimethylpyridine(1073-21-8)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 22-37/38-41
• Safety Statements: 26-39
• HazardClass: 6.1
• Hazardous Substances Data: 1073-21-8(Hazardous Substances Data)

Usage

Uses

3-Amino-2,4-dimethylpyridine is a useful reagent for the synthesis and studies of diazepines and derivatives.

InChI:InChI=1/C7H10N2/c1-5-3-4-9-6(2)7(5)8/h3-4H,8H2,1-2H3

Upstream product

• 89793-08-8 6-chloro-2,4-dimethyl-3-nitropyridine 
• 108-47-4 2,4-lutidine 
• 55314-30-2 2,4-dimethylnicotinic acid 
• 22934-24-3 3-nitro-6-hydroxy-2,4-dimethylpyridine 
• 1074-76-6 2,4-dimethyl-3-nitropyridine 

Downstream Products

• 27296-76-0 2,4-dimethyl-pyridin-3-ol 
• 860411-35-4 7-methyl-3H-pyrazolo[3,4-c]pyridine 
• 1421251-56-0 2-(2,6-diethylphenyl)-6-(2,4-dimethylpyridin-3-yl)-4-methyl-5,6,7,8-tetrahydro(5,5-²H₂)-1,6-naphthyridine 
• 1421254-08-1 2-(2,6-diethylphenyl)-6-(2,4-dimethylpyridin-3-yl)-4-methyl-7,8-dihydro-1,6-naphthyridin-5(6H)-one 
• 1421254-07-0 2-(2,6-diethylphenyl)-6-(2,4-dimethylpyridin-3-yl)-4-methyl-1,6-naphthyridin-5(6H)-one 
• 1417332-55-8 1-(4-Methoxy-phenyl)-3-methyl-6-phenyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid (2,4-dimethyl-pyridin-3-yl)-amide 
• 1417331-93-1 1-(4-Methoxy-phenyl)-3,6-dimethyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid (2,4-dimethyl-pyridin-3-yl)-amide 
• 1345828-49-0 1-(4-fluoro-phenyl)-1H-pyrazolo[3,4-c]pyridine-4-carboxylic acid (2,4-dimethyl-pyridin-3-yl)-amide 
• 897733-12-9 6-bromo-2,4-dimethyl-pyridin-3-amine 
• 143509-33-5 2,4-dimethyl-3-hydroxypyridine N-oxide 

Relevant articles and documents

Synthesis and Antitumor Activity of 3- and 5-Hydroxy-4-methylpyridibe-2-carboxaldehyde Thiosemicarbazones

To develop an α-(N)-heterocyclic carboxaldehyde thiosemicarbazone with clinical utility as an anticancer agent, two analogues, 3-hydroxy-4-methylpyridine-2-carboxaldehyde thiosemicarbazone (3-HMP) and 5-hydroxy-4-methylpyridine-2-carboxaldehyde thiosemicarbazone (5-HMP), of 5-hydroxypyridine-2-carboxaldehyde thiosemicarbazone (5-HP) have been designed and synthesized by two different methods. 3-HMP and 5-HMP both showed better antitumor activity than their respective parent compounds, 3-hydroxypyridine-2-carboxaldehyde thiosemicarbazone and 5-HP, in mice bearing the L1210 leukemia.

Substituted pyridinyl and pyrimidinyl derivatives as modulators of metabolism and the treatment of disorders related thereto

The present invention relates to certain substituted pyridinyl and pyrimidinyl derivatives of Fomula (Ia) that are modulators of metabolism. Accordingly, compounds of the present invention are useful in the treatment of metabolic-related disorders and com

THE EFFECT OF VICINAL METHYL GROUPS ON THE REDUCTION OF AROMATIC NITRO COMPOUNDS WITH LITHIUM ALUMINIUM HYDRIDE

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