1333222-16-4

Basic information

• Product Name: (6-methoxypyrimidine-2,4-diyl)dimethanol
• Synonyms: (6-methoxypyrimidine-2,4-diyl)dimethanol
• CAS NO: 1333222-16-4
• Molecular Formula: C7H10N2O3
• Molecular Weight: 170.1659
• Mol File: 1333222-16-4.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (6-methoxypyrimidine-2,4-diyl)dimethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (6-methoxypyrimidine-2,4-diyl)dimethanol(1333222-16-4)
• EPA Substance Registry System: (6-methoxypyrimidine-2,4-diyl)dimethanol(1333222-16-4)

Safety Data

• Hazardous Substances Data: 1333222-16-4(Hazardous Substances Data)

Usage

Description

(6-Methoxypyrimidine-2,4-diyl)dimethanol is a pyrimidine derivative with the molecular formula C7H10N2O3. It features a heterocyclic ring composed of carbon and nitrogen atoms, along with two methoxy groups and two hydroxyl groups, classifying it as a diol. (6-Methoxypyrimidine-2,4-diyl)dimethanol's unique structural properties lend it potential applications in the pharmaceutical and agrochemical industries, and it may also serve as a building block in the synthesis of other organic compounds.

Uses

Used in Pharmaceutical Industry:
(6-Methoxypyrimidine-2,4-diyl)dimethanol is used as a chemical intermediate for the development of pharmaceutical compounds. Its unique structure allows it to be a key component in the synthesis of various drugs, potentially contributing to the creation of new medications with novel therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, (6-Methoxypyrimidine-2,4-diyl)dimethanol is utilized as a precursor in the synthesis of agrochemicals. Its structural features make it a valuable component in developing new pesticides, herbicides, or other agricultural chemicals that can improve crop protection and yield.
Used in Organic Synthesis:
(6-Methoxypyrimidine-2,4-diyl)dimethanol is used as a building block in the synthesis of other organic compounds. Its presence of methoxy and hydroxyl groups provides versatility in chemical reactions, enabling the creation of a wide range of organic molecules for various applications in research and industry.