CAS 1152617-24-7

2-Amino-3-chloro-4-iodopyridine

Description:

2-Amino-3-chloro-4-iodopyridine is a heterocyclic organic compound characterized by the presence of a pyridine ring substituted with amino, chloro, and iodo groups. The molecular structure features a pyridine backbone, which is a six-membered aromatic ring containing one nitrogen atom. The amino group (-NH2) is typically a strong electron-donating group, enhancing the compound's reactivity and potential for forming hydrogen bonds. The chloro (-Cl) and iodo (-I) substituents introduce halogen atoms that can influence the compound's physical and chemical properties, such as solubility and reactivity. This compound may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its unique combination of functional groups can lead to diverse applications, including in the synthesis of pharmaceuticals or agrochemicals. Additionally, the presence of halogens can affect the compound's stability and interaction with other molecules. As with many chemical substances, safety and handling precautions should be observed due to potential toxicity or reactivity.

Synonyms:

• 3-Chloro-4-Iodopyridin-2-Amine

(3-Chloro-4-iodopyridin-2-yl)amine

CAS: 1152617-24-7

Formula: C₅H₄ClIN₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 254.4561

Ref: IN-DA00962W

3-Chloro-4-iodopyridin-2-amine

CAS: 1152617-24-7

3-Chloro-4-iodopyridin-2-amine

Purity: 98%

Molecular weight: 254.458g/mol

Ref: 54-OR73222

3-CHLORO-4-IODOPYRIDIN-2-AMINE

CAS: 1152617-24-7

Formula: C₅H₄ClIN₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 254.46

Ref: 10-F331932

3-Chloro-4-iodopyridin-2-amine

CAS: 1152617-24-7

3-Chloro-4-iodopyridin-2-amine is a chemical compound with the formula CHI. It is a white solid that can be used in evaluating cross-coupling reactions, such as the coupling of an alkyne with a chlorine atom. This chemical has been shown to react well with chlorination reagents and to form substituted cyanides. The nature of the substituent on the chlorine atom determines its regioselectivity and reactivity, making this compound useful for regiocontrolled synthesis.

Formula: C₅H₄ClIN₂

Purity: Min. 95%

Molecular weight: 254.46 g/mol

Ref: 3D-CWB61724