1194-64-5 | 2-Chloro-6-methylbenzaldehyde

Packsize	Purity	Availability	Price	Discounted Price
250mg	96%	in stock	$15.00	$11.00
1g	96%	in stock	$40.00	$28.00
5g	96%	in stock	$126.00	$88.00
10g	96%	in stock	$214.00	$150.00
25g	96%	in stock	$407.00	$285.00
100g	96%	in stock	$1,536.00	$1,075.00

Description

• Catalog Number: AA24051
• Chemical Name: 2-Chloro-6-methylbenzaldehyde
• CAS Number: 1194-64-5
• Molecular Formula: C8H7ClO
• Molecular Weight: 154.5936
• MDL Number: MFCD01934409
• SMILES: O=Cc1c(C)cccc1Cl

Computed Properties

• Complexity: 124
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2.4

Upstream Synthesis Route

2-Chloro-6-methylbenzaldehyde holds significant importance in chemical synthesis due to its versatile applications. This compound serves as a valuable building block in the creation of a wide range of organic compounds. Its unique chemical structure allows it to participate in various reactions, making it a valuable reagent in the laboratory.One common application of 2-Chloro-6-methylbenzaldehyde is its use as a starting material in the synthesis of pharmaceuticals. The aldehyde group in the molecule can undergo multiple transformations, such as nucleophilic addition and condensation reactions, to introduce specific functional groups required for drug development. This versatility makes it a valuable intermediate in the pharmaceutical industry.Furthermore, 2-Chloro-6-methylbenzaldehyde can also be utilized in the synthesis of agrochemicals and fine chemicals. Its ability to undergo selective reactions allows chemists to modify its structure to introduce desired properties for specific applications. This compound plays a crucial role in designing and producing advanced materials for various industries.Overall, the application of 2-Chloro-6-methylbenzaldehyde in chemical synthesis showcases its versatility and importance as a key building block in the creation of complex organic molecules. Its unique reactivity and ability to participate in diverse reactions make it a valuable tool for chemists in designing and synthesizing a wide range of compounds.