AB44973
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
10g | in stock | $5.00 | $4.00 | - + | ||
25g | in stock | $12.00 | $9.00 | - + | ||
100g | in stock | $39.00 | $28.00 | - + | ||
500g | in stock | $89.00 | $63.00 | - + | ||
1000g | 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.
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 |
Complexity: | 125 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 9 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 1 |
XLogP3: | 1.3 |
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.
Physical chemistry chemical physics : PCCP 20121021
Acta crystallographica. Section E, Structure reports online 20121001
Acta crystallographica. Section E, Structure reports online 20120901
Inorganic chemistry 20120716
Acta crystallographica. Section E, Structure reports online 20120501
Acta crystallographica. Section E, Structure reports online 20120301
International journal of molecular sciences 20120101
Acta poloniae pharmaceutica 20120101
Acta crystallographica. Section E, Structure reports online 20111201
Inorganic chemistry 20110502
Acta crystallographica. Section E, Structure reports online 20101201
Acta crystallographica. Section E, Structure reports online 20101101
Acta crystallographica. Section E, Structure reports online 20100701
Acta crystallographica. Section E, Structure reports online 20100701
Chemical research in toxicology 20100517
Langmuir : the ACS journal of surfaces and colloids 20100504
The journal of physical chemistry. B 20100121
Acta crystallographica. Section E, Structure reports online 20091201
Electrophoresis 20090801
Acta crystallographica. Section E, Structure reports online 20090801
The journal of physical chemistry. A 20090402
Rapid communications in mass spectrometry : RCM 20090101
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20081115
Acta crystallographica. Section E, Structure reports online 20081001
Acta crystallographica. Section E, Structure reports online 20080701
The Journal of chemical physics 20080428
Acta crystallographica. Section E, Structure reports online 20080301
The journal of physical chemistry. A 20080221
Methods in molecular biology (Clifton, N.J.) 20080101
Physical chemistry chemical physics : PCCP 20070314
Inorganic chemistry 20070305
Journal of combinatorial chemistry 20070101
The journal of physical chemistry. A 20061012
Analytical biochemistry 20060701
The journal of physical chemistry. A 20060309
Journal of the American Chemical Society 20060308
The journal of physical chemistry. A 20051215
Chemical & pharmaceutical bulletin 20051001
Journal of the American Chemical Society 20050914
The journal of physical chemistry. A 20050818
Journal of the American Chemical Society 20050518
The journal of physical chemistry. B 20050203
BMC biochemistry 20050101
The Journal of chemical physics 20040808
Journal of the American Chemical Society 20040218
Carbohydrate research 20030523
Se pu = Chinese journal of chromatography 20020501
Hua xi yi ke da xue xue bao = Journal of West China University of Medical Sciences = Huaxi yike daxue xuebao 20020401
Guang pu xue yu guang pu fen xi = Guang pu 20010401