104-52-9 | 1-Chloro-3-phenylpropane

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$14.00	$10.00
25g	98%	in stock	$16.00	$12.00
100g	98%	in stock	$44.00	$31.00
500g	98%	in stock	$114.00	$80.00

Description

• Catalog Number: AB54076
• Chemical Name: 1-Chloro-3-phenylpropane
• CAS Number: 104-52-9
• Molecular Formula: C9H11Cl
• Molecular Weight: 154.6366
• MDL Number: MFCD00001001
• SMILES: ClCCCc1ccccc1
• NSC Number: 16939

Computed Properties

• Complexity: 74.8
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Rotatable Bond Count: 3
• XLogP3: 3.5

Upstream Synthesis Route

3-Phenylpropyl Chloride, also known as benzyl chloropropane, is a versatile chemical compound commonly utilized in organic synthesis due to its reactivity and functional group compatibility. In chemical reactions, 3-Phenylpropyl Chloride serves as a valuable building block in the preparation of various compounds with diverse properties and applications.One key application of 3-Phenylpropyl Chloride lies in its role as a precursor in the synthesis of pharmaceuticals. By introducing 3-Phenylpropyl Chloride into a reaction mixture, chemists can facilitate the formation of complex organic molecules with pharmacological activities. This compound's flexibility allows for the introduction of the phenylpropyl group into drug candidates, influencing their biological interactions and enhancing their therapeutic potential.Additionally, 3-Phenylpropyl Chloride is commonly employed in the synthesis of fragrance compounds and flavoring agents. Its aromatic phenyl group contributes to the creation of pleasant scents and tastes when incorporated into various products. By strategically incorporating 3-Phenylpropyl Chloride into chemical reactions, researchers can design novel aroma compounds and enhance the sensory qualities of consumer goods.Furthermore, 3-Phenylpropyl Chloride finds applications in the preparation of specialty chemicals and organic intermediates. Its alkyl chloride functionality enables selective modifications and functionalization of organic molecules, allowing for the tailoring of chemical structures to meet specific requirements. Chemists leverage the unique reactivity of 3-Phenylpropyl Chloride to access diverse chemical motifs and expand the synthetic toolbox for creating advanced materials and compounds.