886364-94-9

Basic information

• Product Name: 5-Bromo-4-methyl-2-pyridinecarboxaldehyde
• Synonyms: 5-Bromo-4-methyl-2-pyridinecarboxaldehyde;5-BroMo-4-Methylpicolinaldehyde
• CAS NO: 886364-94-9
• Molecular Formula: C₇H₆BrNO
• Molecular Weight: 200
• Mol File: 886364-94-9.mol

Chemical Properties

• Boiling Point: 261℃
• Flash Point: 112℃
• Appearance: /
• Density: 1.577
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 2.19±0.10(Predicted)
• CAS DataBase Reference: 5-Bromo-4-methyl-2-pyridinecarboxaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Bromo-4-methyl-2-pyridinecarboxaldehyde(886364-94-9)
• EPA Substance Registry System: 5-Bromo-4-methyl-2-pyridinecarboxaldehyde(886364-94-9)

Safety Data

• Hazardous Substances Data: 886364-94-9(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
5-Bromo-4-methyl-2-pyridinecarboxaldehyde is used as a building block in organic synthesis for its ability to participate in various chemical reactions due to its aldehyde and bromine functional groups. Its unique structure allows it to be a versatile component in the creation of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 5-Bromo-4-methyl-2-pyridinecarboxaldehyde is utilized as a key intermediate in the development of new drugs. Its presence in drug molecules can potentially enhance their pharmacological properties, such as improving binding affinity to target proteins or modulating their metabolic stability.
Used as a Reagent in Chemical Reactions:
5-Bromo-4-methyl-2-pyridinecarboxaldehyde serves as a reagent in chemical reactions, facilitating the synthesis of other compounds. Its reactivity, stemming from the aldehyde and bromine groups, makes it suitable for use in a range of organic transformations, such as condensation, addition, and substitution reactions.
Used in the Development of New Drug Candidates:
5-Bromo-4-methyl-2-pyridinecarboxaldehyde is explored for its potential in the development of new drug candidates due to its unique structural features. Its incorporation into drug molecules can lead to the discovery of novel therapeutic agents with improved efficacy and selectivity for various medical conditions.
Overall, 5-Bromo-4-methyl-2-pyridinecarboxaldehyde's applications span across multiple industries, primarily due to its distinctive chemical properties and its role as a building block in the synthesis of complex organic compounds and potential drug molecules.

Upstream product

• 941294-57-1 5-bromo-2-iodo-4-methylpyridine 
• 68-12-2 N,N-dimethyl-formamide 
• 3430-26-0 2,5-Dibromo-4-methylpyridine 

Downstream Products

• 1309959-26-9 5-bromo-2-[5-(3,5-dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-4-methyl-pyridine 
• 1309959-28-1 C₂₁H₁₉Cl₂F₃N₂O₃ 
• 1309959-27-0 6-[5-(3,5-Dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-4-methyl-nicotinic acid 

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