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2,5-Dichlorobenzoylacetonitrile

CAS 56719-08-5 · Chlorinated Compound · 2 functional traits · cGMP compliant · Ships from USA in 2-3 days

Chlorinated Compound

2,5-Dichlorobenzoylacetonitrile

Halogenated PharmaceuticalAgrochemicalFine ChemicalChemical ManufacturingResearch
CAS Number 56719-08-5
Category Chlorinated Compound · Nitrile
Origin USA
Compliance cGMP

Questions? Contact our chemistry team:

chemistry@chem-contract.com | +1 (714) 732-8549
In stock — typically ships within 2-3 business days

About 2,5-Dichlorobenzoylacetonitrile

2,5-Dichlorobenzoylacetonitrile (CAS Number: 56719-08-5) is a chloro-substituted intermediate widely used in nucleophilic displacement reactions. ChemContract Research supplies this simple-complexity compound in high purity from our Huntington Beach, California facility, ensuring consistent quality and reliable domestic delivery throughout the United States.

Chloro substituents serve a dual role in drug design — as synthetic handles for late-stage functionalization and as bioisosteres that modulate lipophilicity and binding affinity. The nitrile group is a bioisostere for both carboxylic acids and amides, and has emerged as a covalent warhead in next-generation kinase inhibitors like saxagliptin and neratinib.

Primary applications include nucleophilic aromatic substitution (snar) for ether and amine formation and hydrolysis to carboxylic acids or amides under controlled conditions. This compound serves researchers and manufacturers across the pharmaceutical, agrochemical, fine chemical sectors. Whether you require 2,5-Dichlorobenzoylacetonitrile for early-stage research, process development, or commercial-scale production, ChemContract Research offers flexible ordering from milligram to multi-kilogram quantities with custom synthesis options and full batch documentation including Certificates of Analysis (CoA) and Safety Data Sheets.

Functional Groups: Nitrile (–C≡N)Chlorine (C–Cl)

Chlorinated Compound Applications & Target Industries

How 2,5-Dichlorobenzoylacetonitrile is used across pharmaceutical and agrochemical sectors

01

Nucleophilic aromatic substitution (SNAr) for ether and amine formation

02

Hydrolysis to carboxylic acids or amides under controlled conditions

03

Grignard reagent precursor for C–C bond construction

04

Click chemistry precursor for tetrazole formation (azide–nitrile cycloaddition)

05

Acyl chloride reactivity for amide and ester formation

06

Covalent-warhead cysteine-targeting moiety in kinase inhibitor design

Target Industries: PharmaceuticalAgrochemicalFine ChemicalChemical ManufacturingResearch

2,5-Dichlorobenzoylacetonitrile Specifications

Detailed specifications for this chlorinated compound, including purity, molecular weight, and analytical data are available upon request. Every batch from ChemContract Research includes:

  • Certificate of Analysis (CoA) with purity verification
  • HPLC, NMR, and/or mass spectrometry characterization data
  • Material Safety Data Sheet (MSDS/SDS)
  • Batch-specific documentation and lot traceability
  • Custom analytical testing available on request
Request Full Specifications

Quick Reference

Compound Name 2,5-Dichlorobenzoylacetonitrile
Type Chlorinated Compound
Category Chlorinated Compound · Nitrile
Purity ≥95% (custom grades available)
Complexity Simple (2 functional groups, 0 rings)
Compliance cGMP
Packaging mg to kg scale

Storage & Handling for Chlorinated Compounds

Handling Guidelines

Some chlorinated compounds are volatile or irritating. Use a fume hood and appropriate PPE. Acid chlorides react vigorously with water. Some nitriles may release HCN upon decomposition. Handle in a well-ventilated fume hood with a cyanide antidote kit accessible.

Storage Conditions

Store at recommended temperature in a well-sealed container. Protect from moisture and strong bases. Store in a cool, dry, well-ventilated area. Keep tightly sealed and away from acids and strong bases.

Why Buy 2,5-Dichlorobenzoylacetonitrile From ChemContract?

Quality Assured

Every batch of 2,5-Dichlorobenzoylacetonitrile is produced under cGMP conditions with full CoA documentation, HPLC purity verification, and lot traceability.

Fast USA Shipping

Ship from our Huntington Beach, CA facility with 2-3 business day domestic delivery. No import delays, no customs fees, no tariff surprises.

Custom Synthesis

Need a specific grade, quantity, or derivative of 2,5-Dichlorobenzoylacetonitrile? Our team of PhD chemists can develop custom synthesis solutions for your exact requirements.

Frequently Asked

Common questions about 2,5-Dichlorobenzoylacetonitrile

What is 2,5-Dichlorobenzoylacetonitrile used for? +

2,5-Dichlorobenzoylacetonitrile is a chloro-substituted intermediate widely used in nucleophilic displacement reactions used primarily in the pharmaceutical and agrochemical industries. Key applications include nucleophilic aromatic substitution (snar) for ether and amine formation and hydrolysis to carboxylic acids or amides under controlled conditions.

Where can I buy 2,5-Dichlorobenzoylacetonitrile in the USA? +

ChemContract Research is a trusted USA-based supplier of 2,5-Dichlorobenzoylacetonitrile. We offer competitive pricing, fast domestic shipping from our Huntington Beach, California facility, and full quality documentation including Certificates of Analysis (CoA). Request a quote at chemistry@chem-contract.com or call +1 (714) 732-8549.

What purity levels are available for 2,5-Dichlorobenzoylacetonitrile? +

ChemContract Research supplies 2,5-Dichlorobenzoylacetonitrile in multiple purity grades: ≥95% standard grade, ≥97% high-purity grade, and ≥99% ultra-high-purity grade depending on application requirements. We can also provide custom purity grades through our synthesis capabilities. Contact us for specific purity information and CoA documentation.

Can ChemContract synthesize 2,5-Dichlorobenzoylacetonitrile in custom quantities? +

Yes. ChemContract Research offers custom synthesis services for 2,5-Dichlorobenzoylacetonitrile from milligram to multi-kilogram scale. Our cGMP-compliant facilities and experienced chemists can accommodate custom specifications, packaging requirements, and delivery timelines. Contact our team to discuss your project.

What coupling reactions can I run with 2,5-Dichlorobenzoylacetonitrile? +

As a chlorinated compound, 2,5-Dichlorobenzoylacetonitrile is an excellent substrate for palladium-catalyzed cross-coupling reactions including Suzuki, Heck, Negishi, Sonogashira, and Buchwald–Hartwig amination. It can also be used for Grignard reagent preparation, metal–halogen exchange with organolithium reagents, and nucleophilic substitution reactions.

Can the nitrile group in 2,5-Dichlorobenzoylacetonitrile be converted to other functional groups? +

Yes. The nitrile (–C≡N) in 2,5-Dichlorobenzoylacetonitrile can be hydrolyzed to a carboxylic acid (strong acid/base, heat) or to an amide (milder conditions, e.g., H₂O₂/base). It can be reduced to a primary amine (LiAlH₄ or catalytic hydrogenation), converted to a tetrazole via [3+2] cycloaddition with NaN₃, or used in Grignard additions to form ketones after hydrolysis.

How should I store 2,5-Dichlorobenzoylacetonitrile? +

Store at recommended temperature in a well-sealed container. Protect from moisture and strong bases. Store in a cool, dry, well-ventilated area. Keep tightly sealed and away from acids and strong bases. Always consult the compound-specific Safety Data Sheet (SDS) provided with your order for detailed storage requirements. ChemContract Research includes handling and storage documentation with every shipment.

What is the CAS number of 2,5-Dichlorobenzoylacetonitrile? +

The CAS Registry Number for 2,5-Dichlorobenzoylacetonitrile is 56719-08-5. This unique identifier is used worldwide to reference this specific compound in chemical databases, regulatory filings, and scientific literature. ChemContract Research supplies this compound with full quality documentation. Contact us at chemistry@chem-contract.com for availability and pricing.

Chemical analysis laboratory with HPLC instruments for purity and impurity testing Custom chemical synthesis reaction setup for pharmaceutical intermediate production

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