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Atomfair 3,5-Dichlorobenzaldehyde C7H4Cl2O
Description 3,5-Dichlorobenzaldehyde (CAS No. 10203-08-4) is a high-purity aromatic aldehyde with the molecular formula C7H4Cl2O , widely utilized in organic synthesis and pharmaceutical research. This compound features two chlorine substituents at the 3 and 5 positions of the benzaldehyde ring, enhancing its reactivity in electrophilic substitution and condensation reactions. With a purity of ??98%, it is supplied as a white to off-white crystalline powder, ensuring consistent performance in sensitive applications. Ideal for use as a key intermediate in agrochemicals, dyes, and active pharmaceutical ingredients (APIs), this product is rigorously tested via GC, HPLC, and NMR to meet stringent quality standards.…
Description
Description
3,5-Dichlorobenzaldehyde (CAS No. 10203-08-4) is a high-purity aromatic aldehyde with the molecular formula C7H4Cl2O, widely utilized in organic synthesis and pharmaceutical research. This compound features two chlorine substituents at the 3 and 5 positions of the benzaldehyde ring, enhancing its reactivity in electrophilic substitution and condensation reactions. With a purity of ??98%, it is supplied as a white to off-white crystalline powder, ensuring consistent performance in sensitive applications. Ideal for use as a key intermediate in agrochemicals, dyes, and active pharmaceutical ingredients (APIs), this product is rigorously tested via GC, HPLC, and NMR to meet stringent quality standards. Packaged under inert conditions to prevent degradation, it is suitable for laboratory and industrial-scale applications.
- CAS No: 10203-08-4
- Molecular Formula: C7H4Cl2O
- Molecular Weight: 175.01
- Exact Mass: 173.9639201
- Monoisotopic Mass: 173.9639201
- IUPAC Name: 3,5-dichlorobenzaldehyde
- SMILES: C1=C(C=C(C=C1Cl)Cl)C=O
- Synonyms: 3,5-Dichlorobenzaldehyde, 10203-08-4, Benzaldehyde, 3,5-dichloro-, M74YU7SE79, EINECS 233-499-0
Application
3,5-Dichlorobenzaldehyde serves as a versatile building block in the synthesis of herbicides, fungicides, and pharmaceutical intermediates. Its electron-deficient aromatic ring makes it valuable in Suzuki-Miyaura coupling and other palladium-catalyzed reactions. Researchers also employ it in the preparation of Schiff bases and heterocyclic compounds for antimicrobial studies. Additionally, it is used in the development of liquid crystal materials and specialty dyes due to its stable yet reactive aldehyde group.
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