85989-61-3

Basic information

• Product Name: 5,7-dichloroiMidazo[1,2-c]pyriMidine
• Synonyms: 5,7-dichloroiMidazo[1,2-c]pyriMidine
• CAS NO: 85989-61-3
• Molecular Formula: C₆H₃Cl₂N₃
• Molecular Weight: 188.01412
• Mol File: 85989-61-3.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Density: 1.69±0.1 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 1.91±0.30(Predicted)
• CAS DataBase Reference: 5,7-dichloroiMidazo[1,2-c]pyriMidine(CAS DataBase Reference)
• NIST Chemistry Reference: 5,7-dichloroiMidazo[1,2-c]pyriMidine(85989-61-3)
• EPA Substance Registry System: 5,7-dichloroiMidazo[1,2-c]pyriMidine(85989-61-3)

Safety Data

• Hazardous Substances Data: 85989-61-3(Hazardous Substances Data)

Usage

General Description

5,7-dichloroiMidazo[1,2-c]pyriMidine is a chemical compound with a molecular formula C6H3Cl2N3. It is a heterocyclic compound containing an imidazole ring and two chlorine atoms. This chemical is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It has also been studied for its potential as an antitumor agent due to its ability to inhibit the growth of cancer cells. 5,7-dichloroiMidazo[1,2-c]pyriMidine is a white to off-white powder and is soluble in organic solvents. Its chemical properties and structure make it a valuable building block for the synthesis of various organic compounds.

Upstream product

• 872059-27-3 7-chloro-5-(methylthio)imidazo[1,2-c]pyrimidine 
• 56817-09-5 7-chloroimidazo[1,2-c]pyrimidin-5-ol 

Relevant articles and documents

SYNTHESIS AND CYTOKININ-LIKE ACTIVITY OF 7-CHLORO-IMIDAZO-PYRIMIDINES

Some 5-amino substituted 7-chloro-imidazolpyrimidines and 7-chloro-8-methylthio-imidazopyrimidines were synthesized for further information on the role of the purine ring in cytokinin structure/activity relationships.Their cytokinin-like activity was examined using four different tests; expansion of cucumber etiolatedcotyledons; formation of chlorophyll in etiolated cotyledons of cucumber; preservation of chlorophyll breakdown in sections of barley leaves; inhibition of root growth in intact wheat seedlings.Compounds with imidazopyrimidine ring were generally less active than those with the purine ring, with the exception of the pentenylamino derivatives, which showed an activity comparable with that of the control, kinetin. Key Word Index--7-chloro-imidazopyrimidines; cytokinin activity; chlorophyll retention; leaf expansion; chlorophyll production; root growth inhibition.

SUBSTITUTED IMIDAZOPYRIMIDINES AND TRIAZOLOPYRIMIDINES

The invention relates to substituted imidazopyrimidines and triazolopyrimidines, to methods for the production thereof, and to the use of same for producing medicaments for the treatment and/or prophylaxis of diseases, especially haematological diseases, preferably leucopenia and neutropenia.