118-69-4 | 2,6-Dichlorotoluene

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$26.00	$18.00
25g	98%	in stock	$35.00	$24.00
100g	98%	in stock	$90.00	$63.00
500g	98%	in stock	$198.00	$138.00

Description

• Catalog Number: AI11556
• Chemical Name: 2,6-Dichlorotoluene
• CAS Number: 118-69-4
• Molecular Formula: C7H6Cl2
• Molecular Weight: 161.02854000000002
• MDL Number: MFCD00000576
• SMILES: Clc1cccc(c1C)Cl
• NSC Number: 60722

Computed Properties

• Complexity: 82.9
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• XLogP3: 4.3

Upstream Synthesis Route

1,3-Dichloro-2-methylbenzene, also known as meta-dichlorotoluene, is a versatile chemical compound commonly used in chemical synthesis processes. This compound serves as a crucial building block in the manufacturing of various chemical products due to its unique structure and properties.
In organic synthesis, 1,3-Dichloro-2-methylbenzene is frequently employed as a starting material for the synthesis of more complex organic compounds. Its reactivity allows it to undergo various chemical reactions, such as electrophilic aromatic substitution, which enables the introduction of different functional groups onto the benzene ring. This versatility makes it a valuable intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals.
Furthermore, 1,3-Dichloro-2-methylbenzene is utilized in the synthesis of polymers and resins, where it acts as a monomer or a crosslinking agent. Its presence can modify the properties of the resulting polymer, such as improving thermal stability, chemical resistance, or mechanical strength. Additionally, it can be utilized in the production of dyes, pigments, and fragrances, where its aromatic nature contributes to the desired color or scent.
Overall, the diverse applications of 1,3-Dichloro-2-methylbenzene in chemical synthesis highlight its significance as a key component in various industries, contributing to the creation of a wide range of essential products.

Literature

• Diclomezine: 6-(3,5-dichloro-4-methyl-phen-yl)pyridazin-3(2H)-one.

  Acta crystallographica. Section E, Structure reports online 20101201

• Synthesis and in-vitro antimycobacterial evaluation of 1-(cyclopropyl/2,4-difluorophenyl/tert-butyl)-1,4-dihydro- 8-methyl-6-nitro-4-oxo-7-(substituted secondary amino)quinoline-3-carboxylic acids.

  Archiv der Pharmazie 20090201

• Spectroscopic and electrochemical characterization of an aqua ligand exchange and oxidatively induced deprotonation in diiron complexes.

  Inorganic chemistry 20040308

• Synthesis and biological activity of pyridinium-type acetylcholinesterase inhibitors.

  The Journal of pharmacy and pharmacology 20031001