88368-32-5

Basic information

• Product Name: 10-chloro-7-methyl-7H-pyrimido[5,4-c]carbazole
• CAS NO: 88368-32-5
• Molecular Formula: C₁₅H₁₀ClN₃
• Molecular Weight: 267.713
• Mol File: 88368-32-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 414.1°C at 760 mmHg
• Flash Point: 204.2°C
• Density: 1.41g/cm³
• Vapor Pressure: 4.57E-07mmHg at 25°C
• Refractive Index: 1.738
• CAS DataBase Reference: 10-chloro-7-methyl-7H-pyrimido[5,4-c]carbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 10-chloro-7-methyl-7H-pyrimido[5,4-c]carbazole(88368-32-5)
• EPA Substance Registry System: 10-chloro-7-methyl-7H-pyrimido[5,4-c]carbazole(88368-32-5)

Safety Data

• Hazardous Substances Data: 88368-32-5(Hazardous Substances Data)

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 14 carbon (C) atoms, 9 hydrogen (H) atoms, 1 chlorine (Cl) atom, and 4 nitrogen (N) atoms.

Explanation

This term describes the specific arrangement of atoms and bonds in the compound, which is crucial for understanding its properties and reactivity.

Explanation

A heterocyclic compound is a cyclic compound containing atoms of at least two different elements, in this case, carbon, hydrogen, chlorine, and nitrogen.

Explanation

Carbazoles are a class of organic compounds containing a seven-membered ring system with two nitrogen atoms and three carbon atoms. This compound belongs to this family.

Explanation

The compound contains a chlorine atom attached to the carbazole ring, which can influence its properties and reactivity.

Explanation

A methyl group (CH3) is attached to the carbazole ring, which can also affect the compound's properties and reactivity.

Explanation

Due to its unique structure and properties, this compound may be used in various chemical and pharmaceutical applications, such as drug development or other specialized fields.

Explanation

The compound's properties and reactivity make it a subject of interest for further research, which could lead to new discoveries and applications.

Explanation

Given the compound's unique properties and potential applications, it is recommended that further study be conducted to better understand its reactivity, properties, and potential uses in various fields.

Chemical structure

10-chloro-7-methyl-7H-pyrimido[5,4-c]carbazole

Heterocyclic compound

Yes

Carbazole family

Yes

Chlorine atom

Present

Methyl group

Present

Potential applications

Chemical and pharmaceutical

Reactivity

Of interest for further study

Drug development

Potential use

Further study

Recommended

Upstream product

• 88368-24-5 dihydro-5,6 chloro-10 methyl-7 pyrimidino<5,4-c>carbazole 

Relevant articles and documents

Synthese de Dihydro-6,7 5H-pyrimidinocarbazoles et de 7H-Pyrimidinocarbazoles

The synthesis of 6,7-dihydro-5H-pyrimidinocarbazoles (3) was achived by cyclisation of 1,2,3,4-tetrahydrocarbazol-4-ones with triformamidomethane.The oxydation with potassium permanganate of 6,7-dihydro-5H-pyrimidinocarbazoles gave the 7H-pyrimidinocarbazoles (4).The reactions of the pyrimidinocarbazoles (4a) and (4e) with lithium organic compounds afforded 4-substituted derivatives (6).The structure of the derivatives was determined by (1)H-NMR and Overhauser effect.Keywords - 1,2,3,4-tetrahydrocarbazol-4-one; 6,7-dihydro-5H-pyrimidinocarbazole; 7H-pyrimidinocarbazole; (1)H-NMR; Overhauser effect