CAS 7703-74-4

2,6-bis(bromomethyl)pyridine

Description:

2,6-Bis(bromomethyl)pyridine is an organic compound characterized by its pyridine ring substituted with two bromomethyl groups at the 2 and 6 positions. This compound typically appears as a colorless to light yellow liquid or solid, depending on its purity and form. It is known for its reactivity due to the presence of bromomethyl groups, which can participate in nucleophilic substitution reactions, making it useful in organic synthesis. The compound is soluble in organic solvents such as dichloromethane and chloroform but has limited solubility in water. Its molecular structure contributes to its potential applications in the synthesis of various pharmaceuticals and agrochemicals. Additionally, 2,6-bis(bromomethyl)pyridine may exhibit biological activity, although specific biological properties would depend on the context of its use. As with many brominated compounds, it is important to handle it with care due to potential toxicity and environmental concerns. Proper safety measures should be taken when working with this substance in a laboratory setting.

Formula: C₇H₇Br₂N

InChI: InChI=1/C7H7Br2N/c8-4-6-2-1-3-7(5-9)10-6/h1-3H,4-5H2

SMILES: c1cc(CBr)nc(c1)CBr

2,6-Bis(bromomethyl)pyridine

CAS: 7703-74-4

Formula: C₇H₇Br₂N

Purity: >99.0%(GC)(T)

Color and Shape: White to Almost white powder to crystaline

Molecular weight: 264.95

Ref: 3B-B1936

2,6-Bis(bromomethyl)pyridine

CAS: 7703-74-4

Formula: C₇H₇Br₂N

Purity: 98%

Color and Shape: Solid

Molecular weight: 264.9452

Ref: IN-DA00330T

2,6-Bis(Bromomethyl)Pyridine

CAS: 7703-74-4

2,6-Bis(Bromomethyl)Pyridine

Purity: 98%

Molecular weight: 264.95g/mol

Ref: 54-OR1010144

2,6-Bis(bromomethyl)pyridine

CAS: 7703-74-4

Formula: C₇H₇Br₂N

Purity: 95%

Color and Shape: Solid, White powder

Molecular weight: 264.948

Ref: 10-F226571

2,6-Bis(bromomethyl)pyridine

CAS: 7703-74-4

2,6-Bis(bromomethyl)pyridine (BMP) is a pyridine derivative that is used as a catalyst in organic synthesis. It has been shown to be an effective catalyst for the conversion of picolinic acid to xanthopterin in the presence of sodium. The reactivity of BMP can be attributed to its functionalities and the metal ion that it contains. The reaction mechanism has been studied by computer modelling and molecular modelling techniques. The catalytic rate is determined by intramolecular hydrogen transfer.

Formula: C₇H₇Br₂N

Purity: Min. 95%

Molecular weight: 264.95 g/mol

Ref: 3D-FB74901