1,3-Cyclohexanedione is a cyclic diketone largelly used as a building block in organic synthesis and pharmaceutical intermediates. Also referred to as (Dihydroresorcinol, Hydroresorcinol) by speciality chemical suppliers. 1,3 Cyclohexanedione participates in condensation, alkylation, and cyclization reactions, providing access to heterocyclic scaffolds for drug design and fine chemicals. Cyclohexane-1,3-dione is a cyclohexanedione carrying oxo substituents at positions 1 and 3. This is a beta-diketone and a cyclohexanedione. With its high chemical stability and versatile reactivity make it a preferred precursor in the preparation of CNS-active agents, herbicides, and specialty intermediates. Supplied in technical grade (B2B Advantage) with consistent quality for reproducible synthetic applications. We are among the trusted 1,3-Cyclohexanedione manufacturers and suppliers worldwide, with reliable lead times and global supply capability.
1,3-Cyclohexanedione is a cyclic diketone largelly used as a building block in organic synthesis and pharmaceutical intermediates. Also referred to as (Dihydroresorcinol, Hydroresorcinol) by speciality chemical suppliers. 1,3 Cyclohexanedione participates in condensation, alkylation, and cyclization reactions, providing access to heterocyclic scaffolds for drug design and fine chemicals. Cyclohexane-1,3-dione is a cyclohexanedione carrying oxo substituents at positions 1 and 3. This is a beta-diketone and a cyclohexanedione. With its high chemical stability and versatile reactivity make it a preferred precursor in the preparation of CNS-active agents, herbicides, and specialty intermediates. Supplied in technical grade (B2B Advantage) with consistent quality for reproducible synthetic applications. We are among the trusted 1,3-Cyclohexanedione manufacturers and suppliers worldwide, with reliable lead times and global supply capability.
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Pharmaceutical
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Pharmaceutical Actives & Precursors
Intermediates & Precursors
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Chemical Properties & Specifications
Eye Irritation (Category 2A), Skin Irritation (Category 2), Acute Toxicity: Category 4 (oral)
P280, P305+P351+P338, P261, P264
H302, H315, H319
Used as a key heterocyclic building block for synthesizing pharmaceuticals and fine chemicals.
Participates in reactions to form CNS-active agents, anti-inflammatory compounds, and herbicide precursors.
Serves in Michael addition, Knoevenagel condensation, and alkylation reactions for diverse chemical scaffolds.
Provides structural motifs for medicinal chemistry research in neuroactive and cardiovascular drug candidates.
Used in the preparation of ligands, dyes, and agrochemical intermediates.
Compatible with multiple organic transformations including alkylation and condensation.
Forms key intermediates for heterocyclic compound libraries.
Store at 15–30 °C in a dry, ventilated space
Protect from moisture, sunlight, and strong oxidizers
1 kg, 5 kg, 25 kg sealed HDPE drums or fiberboard containers
2 years under recommended storage conditions; maintain sealed packaging
Palletized, stack ≤2 drums; comply with local chemical transport regulations
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