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AE49686

1017665-60-9 | 1-Methyl-3-(3-methylphenyl)-1h-pyrazol-5-amine

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $68.00 $48.00 -   +
250mg 95% in stock $82.00 $58.00 -   +
1g 95% in stock $273.00 $192.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE49686
Chemical Name: 1-Methyl-3-(3-methylphenyl)-1h-pyrazol-5-amine
CAS Number: 1017665-60-9
Molecular Formula: C11H13N3
Molecular Weight: 187.24102
MDL Number: MFCD06637389
SMILES: Cc1cccc(c1)c1cc(n(n1)C)N

 

Computed Properties
Complexity: 195  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 14  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 1  
XLogP3: 1.9  

 

 

Upstream Synthesis Route
  • BUTTPARK 88\11-91 is a versatile and highly efficient reagent that plays a crucial role in chemical synthesis processes. Its unique properties make it an excellent choice for a wide range of applications in the field of organic chemistry. One prominent application of BUTTPARK 88\11-91 is as a catalyst in various organic reactions, where it facilitates the conversion of reagents into desired products through selective activation of specific functional groups. This reagent is particularly valued for its ability to accelerate reaction rates and improve overall yields, leading to more efficient and cost-effective synthetic routes.Furthermore, BUTTPARK 88\11-91 is often employed in complex molecule synthesis, where its versatile reactivity and compatibility with a variety of substrates make it an invaluable tool for the construction of intricate chemical structures. Its high selectivity and mild reaction conditions enable the precise manipulation of molecular arrangements, facilitating the synthesis of challenging compounds with high purity and yield.Overall, BUTTPARK 88\11-91 stands out as a key component in the toolkit of synthetic chemists, offering unparalleled efficiency and versatility in a wide range of chemical transformations. Its unique properties unlock new opportunities for the design and synthesis of novel molecules, making it an indispensable reagent in modern organic synthesis strategies.
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