926263-13-0

Basic information

• Product Name: 4-amino-N,3-dimethylbenzamide
• Synonyms: 4-amino-N,3-dimethylbenzamide;AKOS BBV-007890;OTAVA-BB 1134990;UKRORGSYN-BB BBV-007890;4-amino-N,3-dimethylbenzamide(SALTDATA: HCl)
• CAS NO: 926263-13-0
• Molecular Formula: C₉H₁₂N₂O
• Molecular Weight: 164.2
• Mol File: 926263-13-0.mol

Chemical Properties

• Boiling Point: 323.995°C at 760 mmHg
• Flash Point: 149.747°C
• Appearance: /
• Density: 1.107g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.574
• CAS DataBase Reference: 4-amino-N,3-dimethylbenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-amino-N,3-dimethylbenzamide(926263-13-0)
• EPA Substance Registry System: 4-amino-N,3-dimethylbenzamide(926263-13-0)

Safety Data

• Hazardous Substances Data: 926263-13-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Research and Development:
4-amino-N,3-dimethylbenzamide is used as a research compound for its potential therapeutic properties. It has been studied for its anti-inflammatory and analgesic effects, making it a candidate for the development of new medications to treat pain and inflammation.
Used in Enzyme Inhibition Studies:
4-amino-N,3-dimethylbenzamide is also used as an inhibitor in enzymatic processes. Its ability to inhibit certain enzymes makes it a valuable tool in understanding enzyme functions and developing drugs that target specific enzymes.
Used in Neurological Disorder Treatment:
4-amino-N,3-dimethylbenzamide has been investigated for its potential role in the treatment of neurological disorders. Its molecular structure and properties suggest that it may have therapeutic benefits for conditions affecting the nervous system.
Used in Cancer Treatment Research:
Additionally, 4-amino-N,3-dimethylbenzamide has been explored for its potential in cancer treatment. Its effects on cellular processes and its interaction with other compounds make it a promising candidate for further research into oncology and cancer therapies.

InChI:InChI=1/C9H12N2O/c1-6-5-7(9(12)11-2)3-4-8(6)10/h3-5H,10H2,1-2H3,(H,11,12)

Upstream product

• 2486-70-6 4-amino 3-methylbenzoic acid 
• 593-51-1 methylamine hydrochloride 
• 74-89-5 methylamine 

Downstream Products

• 1366233-17-1 C₂₅H₂₈N₂O₄ 
• 1618663-43-6 (S)-N,3-dimethyl-4-((5-(2-methylbenzo[d]oxazol-6-yl)-4-((tetrahydrofuran-3-yl)oxy)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)benzamide 
• 1618663-52-7 4-((4-((4-hydroxy-4-methylcyclohexyl)oxy)-5-(2-methylbenzo[d]oxazol-6-yl)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)-N,3-dimethylbenzamide 
• 1618660-00-6 4-((4-(((1r,4r)-4-hydroxy-4-methylcyclohexyl)oxy)-5-(2-methylbenzo[d]oxazol-6-yl)-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)-N,3-dimethylbenzamide 
• 1618660-01-7 4-((4-(((1s,4s)-4-hydroxy-4-methylcyclohexyl)oxy)-5-(2-methylbenzo[d]oxazol-6-yl)-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)-N,3-dimethylbenzamide 
• 1618659-44-1 4-((4-(cyclopentyloxy)-5-(2-methylbenzo[d]oxazol-6-yl)-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)-N,3-dimethylbenzamide 

Relevant articles and documents

SUBSTITUTED PYRROLOPYRIMIDINE COMPOUNDS, COMPOSITIONS THEREOF, AND METHODS OF TREATMENT THEREWITH

Provided herein are Pyrrolopyrimidine Compounds having the following structure: wherein R1, R2, R3, and L are as defined herein, compositions comprising an effective amount of a Pyrrolopyrimidine Compound, and methods for treating or preventing breast cancer, more particularly triple negative breast cancer, comprising administering an effective amount of such Pyrrolopyrimidine Compounds to a subject in need thereof.

Synthesis, structure and insecticidal activity of some novel amides containing N-pyridylpyrazole

A novel series of amides containing N-pyridylpyrazole were designed and synthesized. All of the compounds were characterized and confirmed by IR, 1H NMR, 13C NMR, MS and elemental analysis. The single crystal structure of 9d was determined by X-ray diffraction. The bioassay tests showed that the title compounds exhibited good insecticidal activities against Mythimna separata Walker, diamondback moth and Laphygma exigua Huebner.