89239-35-0

Basic information

• Product Name: 1H-Imidazo(1,2-c)pyrazolo(3,4-e)pyrimidine, 8-ethyl-7,8-dihydro-1,3,5- trimethyl-
• Synonyms: 1H-Imidazo(1,2-c)pyrazolo(3,4-e)pyrimidine, 8-ethyl-7,8-dihydro-1,3,5- trimethyl-;CI 943
• CAS NO: 89239-35-0
• Molecular Formula: C12H17N5
• Molecular Weight: 231.29688
• Mol File: 89239-35-0.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 400.2°C at 760 mmHg
• Flash Point: 195.8°C
• Appearance: /
• Density: 1.34g/cm³
• Vapor Pressure: 1.29E-06mmHg at 25°C
• Refractive Index: 1.698
• CAS DataBase Reference: 1H-Imidazo(1,2-c)pyrazolo(3,4-e)pyrimidine, 8-ethyl-7,8-dihydro-1,3,5- trimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Imidazo(1,2-c)pyrazolo(3,4-e)pyrimidine, 8-ethyl-7,8-dihydro-1,3,5- trimethyl-(89239-35-0)
• EPA Substance Registry System: 1H-Imidazo(1,2-c)pyrazolo(3,4-e)pyrimidine, 8-ethyl-7,8-dihydro-1,3,5- trimethyl-(89239-35-0)

Safety Data

• Hazardous Substances Data: 89239-35-0(Hazardous Substances Data)

Usage

Explanation

The compound's name describes its structure, which includes an imidazo ring fused with a pyrazolo ring and a pyrimidine ring, with specific substitutions.

Explanation

The molecular formula represents the number of carbon (C), hydrogen (H), and nitrogen (N) atoms in the compound, which is 12, 16, and 4, respectively.
3. Heterocyclic Compound

Explanation

The compound is classified as a heterocyclic compound because it contains a ring structure with more than one type of atom, specifically carbon, nitrogen, and others.
4. Imidazo Ring

Explanation

The compound contains an imidazo ring, which is a five-membered ring with two nitrogen atoms and three carbon atoms.
5. Pyrazolo Ring

Explanation

The compound also contains a pyrazolo ring, which is a five-membered ring with one nitrogen atom and four carbon atoms.
6. Pyrimidine Ring

Explanation

The compound has a pyrimidine ring, which is a six-membered ring with four carbon atoms and two nitrogen atoms.
7. Fusion of Rings

Explanation

The imidazo and pyrazolo rings are fused with the pyrimidine ring, creating a complex and unique molecular structure.

Explanation

The compound has an ethyl group (-CH2CH3) attached to the 8th position of the pyrimidine ring, which contributes to its specific properties.

Explanation

The compound is substituted with three methyl groups (-CH3) at the 1st, 3rd, and 5th positions, which further define its structure and properties.
10. Pharmacological Activities

Explanation

Due to its unique structure, the compound may exhibit various pharmacological activities, making it potentially useful in medicinal chemistry.
11. Potential Applications in Medicinal Chemistry

Explanation

The compound's structure and properties suggest that it could be used in the development of new drugs or therapies, particularly in the field of medicinal chemistry.

Substitution at 8th Position

Ethyl Group

Substitution at 1st, 3rd, and 5th Positions

Methyl Groups

InChI:InChI=1/C12H17N5/c1-5-9-6-17-8(3)13-10-7(2)15-16(4)11(10)12(17)14-9/h9H,5-6H2,1-4H3