5-Iodo-4-methyl-pyridin-2-ylamine
5-Iodo-4-methyl-pyridin-2-ylamine (CAS: 356561-08-5), with the molecular formula C6H7IN2 and a molecular weight of 234.04 g/mol, is a halogenated heterocyclic compound. As a key building block, it plays a role in diverse chemical synthesis pathways. This pyridine derivative is valuable for researchers and manufacturers developing novel molecules, particularly within the fields of organic chemistry and materials science.

Organic Synthesis Intermediate
Serves as a crucial intermediate in the synthesis of complex organic molecules. Its unique structure, featuring an iodine substituent and an amino group on a pyridine ring, allows for versatile functionalisation in multi-step reactions.
Pharmaceutical Research
Utilised as a building block in the discovery and development of new pharmaceutical agents. The pyridine scaffold is prevalent in many biologically active compounds, making this iodo-derivative a valuable starting material for medicinal chemistry programmes.
Materials Science
Applicable in the development of advanced materials. Its incorporation into polymer structures or functional materials can impart specific electronic or optical properties, driven by the heteroaromatic system and halogen substituent.
Heterocyclic Chemistry
Essential for constructing diverse heterocyclic systems. Researchers employ this compound to introduce substituted pyridine moieties into larger molecular architectures, expanding the scope of heterocyclic chemistry.
| Molecular weight | 234.04 |
|---|---|
| Empirical formula | C6H7IN2 |
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is 5-Iodo-4-methyl-pyridin-2-ylamine used for?
+
5-Iodo-4-methyl-pyridin-2-ylamine is primarily used as a building block in organic synthesis, particularly in pharmaceutical research and materials science for constructing complex molecules and novel heterocyclic systems.
What are the CAS number and formula for 5-Iodo-4-methyl-pyridin-2-ylamine?
+
The CAS number is 356561-08-5, and the empirical formula is C6H7IN2.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies this chemical as a research grade compound. The specific assay is not detailed in the provided data. TSS does not represent this product as USP, BP, or EP grade.
What are the safety considerations for handling 5-Iodo-4-methyl-pyridin-2-ylamine?
+
Refer to the Safety Data Sheet (SDS) for comprehensive safety information. Handle with appropriate personal protective equipment in a well-ventilated area to avoid exposure.
How is 5-Iodo-4-methyl-pyridin-2-ylamine packed, shipped, and exported?
+
Tech Serve Solutions packs, ships, and exports fine chemicals globally, adhering to all relevant international regulations for hazardous materials transportation.
How can I request a sample or quote for 5-Iodo-4-methyl-pyridin-2-ylamine?
+
Please contact our sales team or use the online form on our website to request a sample or a quotation for 5-Iodo-4-methyl-pyridin-2-ylamine.
▶ Related products

1-(2-Fluorobenzyl)piperazine
C11H15FN2
Chemical Synthesis
1-(2-Fluorophenyl)biguanide hydrochloride
Chemical Synthesis

1-(2-Fluorophenyl)cyclopropanecarboxylic acid
C10H9FO2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine
C10H13FN2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine monohydrochloride
C10H13FN2 · HCl
Chemical Synthesis
1-(2-Furoyl)-1H-benzotriazole
C11H7N3O2
Chemical Synthesis
1-(2-Furoyl)piperazine
C9H12N2O2
Chemical Synthesis
1-(2-Hydroxy-5-methylphenyl)-3-phenyl-1,3-propanedione
Chemical Synthesis
▶ Explore more

3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis

3-Methyl-1,5-pentanediol
Chemical Synthesis

3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis