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Catalog No. RY111041CAS 923590-95-8

4-Bromoisoindoline hydrochloride

In Stock
Purity95%

Molecular Structure

4-Bromoisoindoline hydrochloride chemical structure (CAS 923590-95-8)
Source: PubChem

Pricing & Availability

Pack SizePriceAvailability
100mg$10.00In StockInquire
250mg$12.00In StockInquire
1g$20.00In StockInquire
5g$64.00In StockInquire
10g$115.00In StockInquire
25g$273.00In StockInquire

Total stock: 125g • Ships within 1-2 business days

Specifications

Catalog No.RY111041
CAS No.923590-95-8
Molecular Formula-
Molecular Weight-
Purity95%
SMILESBrC1=CC=CC2=C1CNC2.[H]Cl
MDL NumberMFCD10700134
Categorybuilding-blocks
AvailabilityIn Stock

Synonyms & Alternative Names

4-Bromoisoindoline hydrochloride (IUPAC)Raynchem RY111041

Product Description

4-Bromoisoindoline hydrochloride (CAS 923590-95-8) is a high-quality chemical intermediate offered by Raynchem for pharmaceutical, agrochemical, and material science research. The SMILES notation for 4-Bromoisoindoline hydrochloride is BrC1=CC=CC2=C1CNC2.[H]Cl, representing its complete molecular connectivity for computational chemistry and cheminformatics applications. Our 4-Bromoisoindoline hydrochloride is available with a guaranteed purity of 95%, ensuring consistent and reliable results for your R&D and production needs. Each batch is accompanied by a Certificate of Analysis (COA) verifying identity, purity, and quality. Raynchem provides worldwide fast shipping, competitive pricing, and comprehensive technical support. COA and SDS documents are available upon request. Contact us today for bulk quantities and custom synthesis inquiries.

Applications

  • ●Pharmaceutical Intermediate Synthesis: 4-Bromoisoindoline hydrochloride (CAS 923590-95-8) serves as a versatile building block in the synthesis of active pharmaceutical ingredients (APIs), enabling the construction of complex molecular architectures through palladium-catalyzed cross-coupling reactions such as Suzuki, Buchwald-Hartwig, and Heck reactions.
  • ●Agrochemical Development: This compound is utilized in the preparation of novel agrochemical agents, including herbicides, insecticides, and fungicides, where its halogenated aromatic structure provides key reactivity for further functionalization.
  • ●Material Science Research: 4-Bromoisoindoline hydrochloride is employed in the development of organic electronic materials, coordination polymers, and functional dyes, where its aromatic amine moiety contributes to optoelectronic properties.
  • ●Fine Chemical Manufacturing: 4-Bromoisoindoline hydrochloride is suitable for scale-up from milligram to kilogram quantities, supporting both early-stage discovery and late-stage production needs.

Safety & Handling

Hazard Information

  • !4-Bromoisoindoline hydrochloride may cause mild irritation to skin, eyes, and respiratory tract.
  • !Handle with standard laboratory precautions.
  • !Contains bromine — may release hazardous decomposition products at high temperatures.
  • !Contains nitrogen — handle as a potential irritant and avoid formation of nitrogen oxides.

Precautionary Measures

  • ✓Wear appropriate personal protective equipment (PPE): chemical-resistant gloves, safety goggles, and laboratory coat.
  • ✓Work in a well-ventilated fume hood when handling 4-Bromoisoindoline hydrochloride.
  • ✓Avoid direct contact with skin, eyes, and clothing. Do not breathe dust, vapors, or aerosols.
  • ✓Wash hands thoroughly after handling. Remove contaminated clothing before reuse.

This information is provided as a general guide. Always consult the Safety Data Sheet (SDS) for complete safety information before handling.

Storage & Stability

  • ●4-Bromoisoindoline hydrochloride should be stored in a cool, dry place away from direct sunlight and moisture.
  • ●Keep the container tightly sealed when not in use to prevent degradation and contamination.
  • ●Store separately from incompatible materials such as strong oxidizing agents, acids, and bases.
  • ●Under proper storage conditions, the shelf life of this product is typically 24 months from the date of manufacture.

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