61010-04-6 | 2-Chloro-3-(hydroxymethylene)-1-cyclohexene-1-carboxaldehyde

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$14.00	$10.00
1g	95%	in stock	$29.00	$21.00
5g	95%	in stock	$135.00	$95.00
25g	95%	in stock	$619.00	$433.00
100g	95%	in stock	$2,157.00	$1,510.00

Description

• Catalog Number: AB49371
• Chemical Name: 2-Chloro-3-(hydroxymethylene)-1-cyclohexene-1-carboxaldehyde
• CAS Number: 61010-04-6
• Molecular Formula: C8H9ClO2
• Molecular Weight: 172.6089
• MDL Number: MFCD01863678
• SMILES: OC=C1CCCC(=C1Cl)C=O

Computed Properties

• Complexity: 228
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• Undefined Bond Stereocenter Count: 1
• XLogP3: 1.1

Upstream Synthesis Route

2-Chloro-3-(hydroxymethylene)-1-cyclohexene-1-carboxaldehyde, also known as $name$, is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic chemistry, $name$ serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals.One of the main applications of $name$ is its role as a precursor in the synthesis of heterocyclic compounds. Its cyclohexene ring structure provides a valuable scaffold for the formation of complex molecular structures. By functionalizing the aldehyde and chlorine groups present in $name$, chemists can introduce a variety of substituents to tailor the properties of the final product.$name$ is also commonly employed in the synthesis of chiral compounds. The presence of the hydroxymethylene group offers a unique stereochemical environment that can be utilized in asymmetric catalysis and stereoselective reactions. By carefully designing the synthetic route involving $name$, chemists can access enantiomerically pure compounds with high optical purity.Furthermore, $name$ is utilized in the preparation of building blocks for natural product synthesis. Its ability to undergo diverse transformations, such as aldol condensation, Michael addition, and cycloaddition reactions, makes it a valuable intermediate for accessing structurally complex molecules found in nature.In summary, 2-Chloro-3-(hydroxymethylene)-1-cyclohexene-1-carboxaldehyde plays a crucial role in modern chemical synthesis as a versatile and essential component for the construction of diverse organic compounds with applications in pharmaceuticals, agrochemicals, and beyond.