CAS 1206968-90-2

(5-bro-3-(trifluoroMethyl)pyridine-2-yl)Methanol

Description:

(5-Bromo-3-(trifluoromethyl)pyridine-2-yl)methanol is a chemical compound characterized by its unique structural features, including a pyridine ring substituted with a bromine atom and a trifluoromethyl group. The presence of the bromine atom at the 5-position and the trifluoromethyl group at the 3-position of the pyridine ring significantly influences its chemical reactivity and physical properties. This compound is likely to exhibit polar characteristics due to the hydroxyl (-OH) group, which can engage in hydrogen bonding, enhancing its solubility in polar solvents. The trifluoromethyl group contributes to the compound's lipophilicity and can affect its biological activity, making it of interest in medicinal chemistry. Additionally, the bromine substituent can participate in various chemical reactions, such as nucleophilic substitutions. Overall, this compound's unique combination of functional groups makes it a valuable intermediate in organic synthesis and a potential candidate for further research in pharmaceuticals and agrochemicals.

Formula: C₇H₅BrF₃NO

Synonyms:

• (5-bro-3-(trifluoroMethyl)pyridine-2-yl)Methanol
• 5-Bromo-3-(trifluoromethyl)pyridine-2-methanol
• 2-Pyridinemethanol, 5-bromo-3-(trifluoromethyl)-
• (5-BroMo-3-(trifluoroMethyl)pyridin-2-yl)Methanol
• (5-Bromo-3-(trifluoromethyl)pyridine-2-yl)methanol

(5-bro-3-(trifluoromethyl)pyridine-2-yl)methanol

CAS: 1206968-90-2

Formula: C₇H₅BrF₃NO

Purity: 98%

Color and Shape: Solid

Molecular weight: 256.0199

Ref: IN-DA0095DR

(5-Bromo-3-(trifluoromethyl)pyridin-2-yl)methanol

CAS: 1206968-90-2

(5-Bromo-3-(trifluoromethyl)pyridin-2-yl)methanol

Purity: 98%

Molecular weight: 256.02g/mol

Ref: 54-PC101541

(5-Bromo-3-(trifluoromethyl)pyridin-2-yl)methanol

CAS: 1206968-90-2

Formula: C₇H₅BrF₃NO

Purity: 98%

Color and Shape: No data available.

Molecular weight: 256.022

Ref: 10-F461077

(-)-Isopinocampheol

CAS: 1206968-90-2

(-)-Isopinocampheol is a natural product with the molecular formula C(14)H(28)O. It is extracted from various plants, such as "Erythroxylum coca" and "Psychotria viridis". (-)-Isopinocampheol is a chiral molecule that has been shown to have reactivity in the synthesis of other natural products. (-)-Isopinocampheol can be alkylated at the 2-position with chloromethyl methyl ether. This reaction yields an intermediate that undergoes β-elimination, forming a piperidine skeleton. (-)-Isopinocampheol has been evaluated as a potential anti-cancer drug candidate due to its ability to inhibit proliferation of tumor cells in culture. The mechanism of action is not yet clear, but may involve inhibition of protein synthesis or induction of apoptosis.

Formula: C₁₀H₁₈O

Purity: Min. 95%

Molecular weight: 154.24 g/mol

Ref: 3D-GYB96890