5-BROMO-2-CHLORO-4-PICOLINE

Product Name:5-BROMO-2-CHLORO-4-PICOLINE
CAS:778611-64-6
MFC6H5BrClN
MW:206.47
EINECS:689-064-4
MOL File:778611-64-6.mol

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1. Product Overview & Specifications

5-Bromo-2-chloro-4-picoline (CAS: 778611-64-6) is a halogenated pyridine derivative with the molecular formula C6H5BrClN and a molecular weight of 206.47 g/mol. It is also known as 2-chloro-4-methyl-5-bromopyridine or 5-bromo-2-chloro-4-methylpyridine. This compound is widely utilized as a versatile intermediate in pharmaceutical and agrochemical synthesis.

Specification Comparison

Parameter 5-Bromo-2-chloro-4-picoline Similar Derivatives
CAS Number 778611-64-6 Varies by structure
Molecular Formula C6H5BrClN Depends on substituents
Purity ≥98% (HPLC) Typically 95-99%
Storage 2-8°C in inert atmosphere Similar requirements

2. Key Applications

  • Pharmaceutical Intermediate: Used in synthesizing active pharmaceutical ingredients (APIs) for antiviral and anticancer therapies.
  • Agrochemicals: Key building block for herbicides and fungicides due to its halogenated pyridine backbone.
  • Material Science: Facilitates the production of specialty polymers and liquid crystals.
  • Research & Development: Serves as a precursor for novel heterocyclic compounds in organic chemistry.

3. Usage Guidelines

Handling Precautions

  • Use personal protective equipment (PPE) including gloves, goggles, and lab coats.
  • Avoid inhalation or direct contact with skin/eyes.
  • Store in tightly sealed containers under nitrogen or argon to prevent degradation.

Synthetic Protocols

Typical synthesis involves halogenation of 4-methylpyridine derivatives. A common route includes:

  1. Bromination of 2-chloro-4-picoline using N-bromosuccinimide (NBS) under controlled conditions.
  2. Purification via column chromatography or recrystallization.

4. Industry Case Studies

Case 1: Pharmaceutical Manufacturer (Shanghai)

A leading API producer integrated 5-bromo-2-chloro-4-picoline into their synthesis of a tyrosine kinase inhibitor, achieving a 22% yield improvement compared to traditional intermediates.

Case 2: Agrochemical Innovator (Germany)

Used this compound to develop a next-generation fungicide with enhanced bioavailability, reducing application frequency by 40% in field trials.

Case 3: Research Institute (USA)

Leveraged the compound’s reactivity to create a novel class of fluorescent probes for cellular imaging, published in ACS Chemical Biology (2023).

5. Contact for Inquiries

For technical specifications, bulk pricing, or collaboration opportunities:

Contact Method Details
Email info@vivalr.com
Phone (86) 15866781826
Lead Time 2-4 weeks (custom synthesis available)
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