59797-06-7

Basic information

• Product Name: 1,3,7-trimethylpyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione
• Synonyms: 1,3,7-Trimethylpyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione; pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione, 1,3,7-trimethyl-; TCMDC-123937
• CAS NO: 59797-06-7
• Molecular Formula: C₁₀H₁₁N₃O₂
• Molecular Weight: 205.2132
• Mol File: 59797-06-7.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 364.2°C at 760 mmHg
• Flash Point: 174.1°C
• Density: 1.275g/cm³
• Vapor Pressure: 1.71E-05mmHg at 25°C
• Refractive Index: 1.58
• CAS DataBase Reference: 1,3,7-trimethylpyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,7-trimethylpyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione(59797-06-7)
• EPA Substance Registry System: 1,3,7-trimethylpyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione(59797-06-7)

Safety Data

• Hazardous Substances Data: 59797-06-7(Hazardous Substances Data)

Usage

Classification

Natural stimulant and psychoactive drug

Occurrence

Commonly found in coffee, tea, and energy drinks

Mechanism of Action

Blocks the action of the neurotransmitter adenosine, which promotes relaxation and sleep

Effects

Increased alertness, improved cognitive function, and reduced fatigue

Additional Properties

Diuretic properties, making it a common ingredient in weight loss supplements

Potential Side Effects

Anxiety, palpitations, and insomnia due to excessive consumption

Popularity

Widely consumed and enjoyed for its stimulating effects

Upstream product

• 115893-52-2 1,3,7-trimethyl-2,4-dioxo-1,2,3,4-tetrahydro-pyrido[2,3-d]pyrimidine-5-carboxylic acid 
• 67-64-1 acetone 
• 36980-91-3 1,3-dimethyl-5-cyanouracil 
• 54947-92-1 morpholino-2 propene 
• 181465-38-3 6-amino-1,3-dimethyl-5-thioformyluracil 
• 6972-27-6 1,3-Dimethyl-6-chlorouracil 
• 22412-89-1 cycloocta-2,4,6-trien-1-one 
• 99747-54-3 1,3-dimethyl-2,4-dioxo-6-<(triphenylphosphoranylidene)amino>-1,2,3,4-tetrahydropyrimidine 
• 64-19-7 acetic acid 
• 6642-31-5 6-Amino-1,3-dimethylbarbituric acid 
• 88628-96-0 1,3-dimethyl-6-(α-methylallyl)aminouracil 
• 78-94-4 methyl vinyl ketone 
• 17743-04-3 1,3-dimethyl-6-iminouracil 

Relevant articles and documents

On the reactions of 6-phosphoranylideneaminouracils and related 6-aminouracils with 2,4,6-cyclooctatrienone: Reactions of the intermediates of uracil-annulated 8-azabicyclo[5.3.1]Undecatetraene ring systems

The reaction of 1,3-dimethyl-6-phosphoranylideneaminouracil (4) with 2,4,6-cyclooctatrienone (7) in AcOH gives an intermediacy of uracil-annulated 8-azabicyclo[5.3.1]undeca-2,4,7,9-tetraene (9), which results in the formation of 9-acetoxy-5a, 10-methano-2

Reactivity of Thioaldehyde: Cyclization Reaction of 6-Amino-1,3-dimethyl-5-thioformyluracil with Enamines into Pyridopyrimidine-2,4-(1H,3H)-diones

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Pyrimidines. 21. Novel reactions of 5-cyano-1,3-dimethyluracil with carbon nucleophiles. A facile preparation of certain pyrido[2,3-d]pyrimidines [1]

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