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Home  > Chemistry  > Organic Building Blocks  > Alkynyls  > N4-(3-Ethynylphenyl)-7-methoxyquinazoline-4,6-diamine

AA04916

1012057-52-1 | N4-(3-Ethynylphenyl)-7-methoxyquinazoline-4,6-diamine

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% 1 week $31.00 $22.00 -   +
250mg 97% 1 week $52.00 $37.00 -   +
1g 97% 1 week $139.00 $98.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA04916
Chemical Name: N4-(3-Ethynylphenyl)-7-methoxyquinazoline-4,6-diamine
CAS Number: 1012057-52-1
Molecular Formula: C17H14N4O
Molecular Weight: 290.3193
MDL Number: MFCD16877567
SMILES: COc1cc2ncnc(c2cc1N)Nc1cccc(c1)C#C

 

Computed Properties
Complexity: 420  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 22  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 4  
XLogP3: 3  

 

 

Upstream Synthesis Route
  • N4-(3-Ethynylphenyl)-7-methoxyquinazoline-4,6-diamine, often referred to as $name$, is a versatile compound that finds extensive utility in chemical synthesis. This compound serves as a key building block in the preparation of various advanced materials and pharmaceutical intermediates. In chemical synthesis, $name$ is commonly employed as a crucial reagent due to its unique structural properties. Its ethynyl group enables it to participate in alkyne chemistry, facilitating the introduction of functional groups and the formation of intricate molecular structures. Additionally, the quinazoline moiety in $name$ imparts specific reactivity, allowing for diverse synthetic pathways and the synthesis of heterocyclic compounds.Moreover, the presence of the methoxy group in $name$ can further enhance its chemical reactivity, influencing its solubility and interaction with other molecules during synthesis processes. This feature is particularly valuable in the design of novel molecules with desired properties.Overall, the application of N4-(3-Ethynylphenyl)-7-methoxyquinazoline-4,6-diamine in chemical synthesis underscores its significance as a valuable tool for organic chemists and researchers seeking to access complex molecular architectures and functional materials efficiently and effectively.
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