CAS 1618-47-9

Pyridazine, 3-iodo-6-methyl-

Description:

Pyridazine, 3-iodo-6-methyl- is a heterocyclic organic compound characterized by a pyridazine ring, which consists of two adjacent nitrogen atoms within a six-membered ring of carbon atoms. The presence of an iodine atom at the 3-position and a methyl group at the 6-position contributes to its unique chemical properties. This compound is typically a colorless to pale yellow liquid or solid, depending on its state at room temperature. It is known for its potential applications in pharmaceuticals and agrochemicals due to the reactivity of the iodine substituent, which can participate in various chemical reactions, including nucleophilic substitutions. Pyridazine derivatives often exhibit biological activity, making them of interest in medicinal chemistry. The compound's molecular structure influences its solubility, stability, and reactivity, which are important factors in its practical applications. Safety data should be consulted for handling and storage, as halogenated compounds can pose health risks.

Formula: C₅H₅IN₂

Synonyms:

• 3-Iodo-6-methylpyridazine
• Pyridazine, 3-iodo-6-Methyl-

Pyridazine, 3-iodo-6-methyl-

CAS: 1618-47-9

Formula: C₅H₅IN₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 220.0111

Ref: IN-DA001VX1

3-Iodo-6-methylpyridazine

CAS: 1618-47-9

3-Iodo-6-methylpyridazine

Purity: 98%

Color and Shape: Solid

Molecular weight: 220.01107g/mol

Ref: 54-OR20044

3-Iodo-6-methylpyridazine

CAS: 1618-47-9

Formula: C₅H₅IN₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 220.013

Ref: 10-F464740

3-iodo-6-methylpyridazine

CAS: 1618-47-9

3-Iodo-6-methylpyridazine is an isoquinoline derivative. It is a cross-coupling reagent that can be used as a nucleophile in organic synthesis. 3-Iodo-6-methylpyridazine is a threefold equivalent of the starting material and can be used to synthesize functionalized imines, such as those found in pyrimidine or purine nucleosides. Alkoxycarbonyl groups are common substituents on the pyridine ring of 3-iodo-6-methylpyridazine, which can be used to synthesize substituted pyrimidine or purine nucleosides by coupling with amines. The diethyl ester group on 3-iodo-6-methylpyridazine allows it to be easily converted into other functionalities, such as those found in amino acids. Palladium catalysis has been shown to enhance the yields of this reaction. This re

Formula: C₅H₅N₂I

Purity: Min. 95%

Molecular weight: 220.01 g/mol

Ref: 3D-BAA61847