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Home  > 5-Amino-2-methylbenzotrifluoride

AB67937

65934-74-9 | 5-Amino-2-methylbenzotrifluoride

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $10.00 $7.00 -   +
5g 98% in stock $16.00 $12.00 -   +
10g 98% in stock $28.00 $19.00 -   +
25g 98% in stock $37.00 $26.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB67937
Chemical Name: 5-Amino-2-methylbenzotrifluoride
CAS Number: 65934-74-9
Molecular Formula: C8H8F3N
Molecular Weight: 175.151
MDL Number: MFCD01631582
SMILES: Nc1ccc(c(c1)C(F)(F)F)C

 

Computed Properties
Complexity: 155  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
XLogP3: 2.5  

 

 

Upstream Synthesis Route
  • 4-Methyl-3-(trifluoromethyl)aniline, also known as $name$, is a versatile compound widely utilized in chemical synthesis for its unique properties and functions. As a substituted aniline derivative, $name$ plays a crucial role in diverse organic reactions and transformations. One key application of 4-Methyl-3-(trifluoromethyl)aniline is its use as a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. By serving as a vital intermediate in the production of various compounds, $name$ enables the creation of structurally complex and biologically active molecules with enhanced properties. Additionally, its trifluoromethyl group imparts distinct chemical and physical characteristics, enhancing the overall functionality and performance of the resulting products. In synthesis, 4-Methyl-3-(trifluoromethyl)aniline acts as a versatile reagent for the introduction of the trifluoromethyl moiety into organic frameworks, enabling the development of novel compounds with tailored properties and applications. Its strategic use in chemical transformations underscores its significance as a valuable tool for synthetic chemists and researchers exploring innovative pathways in drug discovery, materials science, and agrochemical development.
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