
Catalog Number	AR00I5QQ
Chemical Name	1(2H)-Naphthalenone, 6-chloro-3,4-dihydro-
CAS Number	26673-31-4
Molecular Formula	C10H9ClO
Molecular Weight	180.6309
MDL Number	MFCD04114377
SMILES	Clc1ccc2c(c1)CCCC2=O

6-Chloro-3,4-dihydronaphthalen-1(2H)-one, also known as $name$, serves as a versatile building block in chemical synthesis due to its unique structural features and reactivity. This compound is widely used in organic synthesis, particularly in the pharmaceutical industry, for the development of various biologically active molecules.1. Key Intermediate: $name$ can be utilized as a key intermediate in the synthesis of pharmaceutical compounds and agrochemicals. Its chloro-substituted naphthalene ring provides a point of diversification for further functional group manipulations.2. Heterocyclic Ring Formation: The chlorine atom in 6-Chloro-3,4-dihydronaphthalen-1(2H)-one can be selectively replaced with nucleophiles to introduce different functional groups. This substitution reaction is common in the formation of heterocycles such as pyrroles, pyrazoles, and indoles.3. Ring-Closing Reactions: The presence of a carbonyl group adjacent to the chlorine atom in $name$ makes it a suitable substrate for ring-closing reactions, enabling the synthesis of cyclic compounds. This feature is valuable in the construction of macrocycles and complex natural products.4. Pharmacophore Modification: Chemists can modify the structure of $name$ by substituting the chlorine atom with various functional groups to fine-tune the compound’s pharmacological properties. This strategy is crucial in structure-activity relationship (SAR) studies for drug discovery.5. Cross-Coupling Reactions: 6-Chloro-3,4-dihydronaphthalen-1(2H)-one can participate in cross-coupling reactions with different coupling partners, including organometallic reagents, to form C–C bonds. This reactivity broadens the scope of reactions available for synthetic transformations.6. Fragment Assembly: By incorporating $name$ into a synthetic route, chemists can efficiently build complex molecular frameworks through fragment assembly strategies. This compound’s ability to undergo diverse chemical transformations enhances the efficiency of multi-step syntheses.In summary, 6-Chloro-3,4-dihydronaphthalen-1(2H)-one plays a pivotal role in chemical synthesis by facilitating the construction of diverse organic molecules through functional group manipulations, ring-closing reactions, and cross-coupling processes. Its utility in pharmaceutical synthesis and heterocyclic chemistry underscores its importance as a valuable building block for the creation of novel compounds with biological activities.

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GHS Pictogram
Signal Word	Warning
UN#	N/A
Hazard Statements	H302-H315-H319-H335
Precautionary Statements	P261-P305+P351+P338
Class	N/A
Packing Group	N/A

Packsize	Purity	Price	Availability
100mg	97%	$5.00	Global Stock	Buy Now	Add To Cart
250mg	97%	$5.00	Global Stock	Buy Now	Add To Cart
1g	97%	$6.00	Global Stock	Buy Now	Add To Cart
5g	97%	$20.00	Global Stock	Buy Now	Add To Cart
10g	97%	$32.00	Global Stock	Buy Now	Add To Cart
25g	97%	$76.00	Global Stock	Buy Now	Add To Cart

1(2H)-Naphthalenone, 6-chloro-3,4-dihydro-