5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine

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Product Specifications & Comparative Analysis

Key Parameters

CAS Number Molecular Formula Molecular Weight Density Boiling Point
22276-95-5 C6H3BrClN3 232.47 g/mol 2.0±0.1 g/cm³ 384.3°C

Comparative Analysis with Derivatives

Variant CAS Number Molecular Weight Key Functional Groups
5-Bromo-4-chloro-7-methyl 1266343-30-9 246.49 g/mol Methyl substitution at 7-position
4-Chloro-7H-pyrrolo(2,3-d)pyrimidine 3680-69-1 153.57 g/mol Absence of bromine substituent

Detailed Applications

Pharmaceutical Intermediates

This compound serves as a critical precursor in synthesizing kinase inhibitors, particularly for oncology therapeutics. Its halogenated structure enables selective binding to ATP pockets in target enzymes.

Agrochemical Research

Used in developing next-generation herbicides due to its stable heterocyclic framework, which enhances metabolic resistance in crop protection formulations.

Operational Guidelines

Storage Protocols

  • Store at 2-8°C under inert atmosphere (Ar/N2)
  • Protect from light in amber glass containers

Reaction Optimization

For Suzuki coupling reactions: Use 1.2 eq Pd(PPh3)4 catalyst in degassed THF/H2O (3:1) at 80°C for 12 hours. Typical yields exceed 78%.

Industry Case Studies

Case 1: Oncology Drug Development

A Shanghai-based pharmaceutical company utilized this intermediate in synthesizing third-generation BTK inhibitors, achieving 92% purity after crystallization.

Case 2: Agricultural Formulation

Beijing researchers incorporated derivatives into novel fungicides, demonstrating 98% efficacy against Puccinia striiformis in field trials.

Contact for Technical Consultation

For bulk pricing, SDS documentation, or custom synthesis requirements:

Email: info@vivalr.com
Tel: (86) 15866781826

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