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AB44544

108-41-8 | 3-Chlorotoluene

Packsize Purity Availability Price Discounted Price    Quantity
25g 98%(GC) in stock $25.00 $18.00 -   +

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Description
Catalog Number: AB44544
Chemical Name: 3-Chlorotoluene
CAS Number: 108-41-8
Molecular Formula: C7H7Cl
Molecular Weight: 126.5835
MDL Number: MFCD00000595
SMILES: Cc1cccc(c1)Cl
NSC Number: 8767

 

Computed Properties
Complexity: 70.8  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 8  
XLogP3: 3.3  

 

 

Upstream Synthesis Route
  • 3-Chlorotoluene, also known as 1-chloro-3-methylbenzene, is a versatile chemical compound frequently utilized in chemical synthesis processes. This compound serves as a key intermediate in the production of various chemicals and pharmaceuticals due to its unique properties and reactivity.One of the primary applications of 3-Chlorotoluene in chemical synthesis is its role as a precursor in the synthesis of important organic compounds such as pharmaceuticals, dyes, and pesticides. This compound can undergo various chemical reactions, including halogenation, nitration, and oxidation, to yield a wide range of derivatives with diverse functionalities.In organic chemistry, 3-Chlorotoluene can be used as a starting material for the synthesis of substituted benzene derivatives through further functional group transformations. By introducing different functional groups onto the aromatic ring of 3-Chlorotoluene, chemists can access a myriad of structurally complex molecules with valuable properties for various applications.Furthermore, 3-Chlorotoluene can also be employed in the synthesis of polymers and industrial chemicals, where its reactivity and compatibility with other compounds make it a valuable building block in the production of specialized materials.Overall, the application of 3-Chlorotoluene in chemical synthesis extends to the creation of a diverse array of compounds that are essential in industries such as pharmaceuticals, materials science, and agrochemicals. Its versatile nature and ability to undergo various chemical transformations make it an indispensable component in the toolkit of synthetic chemists.
Literature
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