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AB44973

873-74-5 | 4-Aminobenzonitrile

Packsize Purity Availability Price Discounted Price    Quantity
10g 98% in stock $5.00 $4.00 -   +
25g 98% in stock $12.00 $9.00 -   +
100g 98% in stock $39.00 $28.00 -   +
500g 98% in stock $89.00 $63.00 -   +
1000g 98% in stock $138.00 $97.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB44973
Chemical Name: 4-Aminobenzonitrile
CAS Number: 873-74-5
Molecular Formula: C7H6N2
Molecular Weight: 118.1359
MDL Number: MFCD00007821
SMILES: N#Cc1ccc(cc1)N
NSC Number: 7625

 

Computed Properties
Complexity: 125  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
XLogP3: 1.3  

 

 

Upstream Synthesis Route
  • 4-Aminobenzonitrile, also known as 4-aminobenzonitrile or p-aminobenzonitrile, is a versatile chemical compound widely used in chemical synthesis. This aromatic amine derivative plays a crucial role in the pharmaceutical and agrochemical industries, as well as in the development of advanced materials and dyes.In chemical synthesis, 4-Aminobenzonitrile serves as a valuable building block for the preparation of various important compounds. One of its key applications is in the synthesis of pharmaceutical intermediates and active pharmaceutical ingredients (APIs). By utilizing 4-Aminobenzonitrile as a starting material, chemists can efficiently access a wide range of heterocyclic compounds and functionalized aromatic derivatives that exhibit biological activity.Furthermore, 4-Aminobenzonitrile is commonly employed in the development of agrochemicals, specifically in the synthesis of herbicides, insecticides, and fungicides. Its structural versatility allows for the modification of key functional groups, enabling the creation of potent crop protection agents with improved efficacy and selectivity.Additionally, 4-Aminobenzonitrile finds application in the field of materials science for the production of specialty polymers, elastomers, and resins. Its ability to undergo various chemical reactions, such as nucleophilic substitutions and condensation reactions, enables the generation of tailored macromolecules with desirable properties, such as thermal stability, mechanical strength, and chemical resistance.Overall, the versatile nature of 4-Aminobenzonitrile makes it a valuable building block in chemical synthesis, facilitating the creation of diverse compounds with applications spanning the pharmaceutical, agrochemical, and materials industries.
Literature
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