262353-35-5

Basic information

• Product Name: Pyrimidine, 2-iodo-4-methoxy- (9CI)
• Synonyms: Pyrimidine, 2-iodo-4-methoxy- (9CI)
• CAS NO: 262353-35-5
• Molecular Formula: C₅H₅IN₂O
• Molecular Weight: 236.01047
• Product Categories: PYRIMIDINE;Heterocycle-Pyrimidine series
• Mol File: 262353-35-5.mol

Chemical Properties

• Boiling Point: 318.793ºC at 760 mmHg
• Flash Point: 146.601ºC
• Appearance: /
• Density: 1.935g/cm3
• Vapor Pressure: 0.001mmHg at 25°C
• Refractive Index: 1.605
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: 0.35±0.20(Predicted)
• CAS DataBase Reference: Pyrimidine, 2-iodo-4-methoxy- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Pyrimidine, 2-iodo-4-methoxy- (9CI)(262353-35-5)
• EPA Substance Registry System: Pyrimidine, 2-iodo-4-methoxy- (9CI)(262353-35-5)

Safety Data

• Hazardous Substances Data: 262353-35-5(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
Pyrimidine, 2-iodo-4-methoxy(9CI) is used as a key intermediate in the synthesis of various pharmaceutical and agrochemical compounds. Its unique structural properties and reactivity make it a valuable building block for the development of new drugs and materials.
Used in Organic Chemistry:
In the field of organic chemistry, Pyrimidine, 2-iodo-4-methoxy(9CI) serves as a crucial component in the preparation of more complex molecules. Its presence in the synthesis process allows for the creation of a wide range of chemical entities with diverse applications.
Used in Drug Development:
Pyrimidine, 2-iodo-4-methoxy(9CI) has potential applications in the development of new drugs due to its structural properties and reactivity. It can be utilized in the design and synthesis of novel therapeutic agents, contributing to advancements in medicine and healthcare.
Used in Material Science:
Pyrimidine, 2-iodo-4-methoxy(9CI) also finds use in material science, where it can be incorporated into the development of new materials with specific properties. Its unique structure and reactivity make it a promising candidate for creating innovative materials with applications in various industries.

InChI:InChI=1/C5H5IN2O/c1-9-4-2-3-7-5(6)8-4/h2-3H,1H3

Upstream product

• 67-56-1 methanol 
• 262353-34-4 2,4‐diiodopyrimidine 
• 22536-63-6 2-chloro-4-methoxypyrimidine 

Downstream Products

• 463337-53-3 1-(4-methoxy-2-pyrimidinyl)ethanone 
• 24903-69-3 4-methoxy-2-trifluoromethylpyrimidine 
• 1644057-87-3 C₁₂H₉F₃N₂O 
• 1644057-86-2 C₁₂H₁₂N₂O₂ 
• 1644057-85-1 4-methoxy-2-(4-methoxyphenyl)pyrimidine 
• 33630-20-5 2-phenyl-4-methoxypyrimidine 

Relevant articles and documents

Synthesis of mono- and diaza-'pyridones' via stille coupling of alkoxystannanes

Various alkoxy-substituted heterocyclic stannanes provide access to the corresponding substituted 'pyridone' moieties via Stille cross-coupling. Both pyridyl and a series of diazinyl stannanes are prepared, and options for unmasking (via demethylation or debenzylation) of the pyridone unit are evaluated. Georg Thieme Verlag Stuttgart. New York.

PIPERDINE COMPOUNDS AND USES THEREOF-911

Compounds of formula (I) and their pharmaceutically acceptable salts are described. Processes for their preparation, pharmaceutical compositions containing them, their use as medicaments and their use in the treatment of bacterial infections are also described.

First study of syntheses and reactivity of Grignard compounds in the diazine series. Diazines. Part 27

A preparation of Grignard derivatives of diazines is described using a halogen magnesium exchange reaction. This convenient method allows the functionalization of these rings at 0°C or even room temperature.