933703-03-8

Basic information

• Product Name: 4-chloropyrimidine-5-carbaldehyde
• Synonyms: 4-chloropyrimidine-5-carbaldehyde
• CAS NO: 933703-03-8
• Molecular Formula: C5H3ClN2O
• Molecular Weight: 142.54
• Mol File: 933703-03-8.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-chloropyrimidine-5-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 4-chloropyrimidine-5-carbaldehyde(933703-03-8)
• EPA Substance Registry System: 4-chloropyrimidine-5-carbaldehyde(933703-03-8)

Safety Data

• Hazardous Substances Data: 933703-03-8(Hazardous Substances Data)

Usage

Description

4-chloropyrimidine-5-carbaldehyde is a chemical compound with the molecular formula C5H3ClN2O. It is a derivative of pyrimidine and is an aldehyde compound with a chlorine substituent. This versatile compound is known for its unique structure and properties, making it a promising candidate for various applications across different industries.

Uses

Used in Pharmaceutical Industry:
4-chloropyrimidine-5-carbaldehyde is used as a building block for the synthesis of pharmaceuticals. Its unique structure allows it to be a key intermediate in the production of various organic compounds, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 4-chloropyrimidine-5-carbaldehyde serves as a crucial component in the synthesis of agrochemicals. Its role as a building block aids in the creation of effective pesticides, herbicides, and other agricultural chemicals that enhance crop protection and yield.
Used in Material Science:
4-chloropyrimidine-5-carbaldehyde is utilized in the development of new materials due to its reactive nature and potential to form various organic compounds. Its application in material science can lead to the creation of innovative products with improved properties and performance.
Used in Chemical Reactions:
As an intermediate, 4-chloropyrimidine-5-carbaldehyde plays a significant role in various chemical reactions. Its versatility allows it to participate in a wide range of processes, enabling the synthesis of diverse organic compounds for multiple applications.