CAS 1885-29-6
:2-Aminobenzonitrile
Description:
2-Aminobenzonitrile, with the CAS number 1885-29-6, is an organic compound characterized by the presence of both an amino group (-NH2) and a nitrile group (-C≡N) attached to a benzene ring. This compound is a derivative of aniline, where the amino group is positioned ortho to the nitrile group on the aromatic ring. It typically appears as a white to light yellow solid and is soluble in polar organic solvents. 2-Aminobenzonitrile is known for its utility in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals. The presence of both functional groups allows for diverse reactivity, making it a valuable intermediate in chemical reactions such as nucleophilic substitutions and coupling reactions. Additionally, it may exhibit biological activity, which has been the subject of research in medicinal chemistry. Proper handling and storage are essential due to its potential toxicity and the need for safety precautions when working with nitriles and amines.
Formula:C7H6N2
InChI:InChI=1S/C7H6N2/c8-5-6-3-1-2-4-7(6)9/h1-4H,9H2
InChI key:InChIKey=HLCPWBZNUKCSBN-UHFFFAOYSA-N
SMILES:C(#N)C1=C(N)C=CC=C1
Synonyms:- 1-Amino-2-cyanobenzene
- 2-Aminobenzonitrile
- 2-Cyananiline
- 2-Cyano-1-aminobenzene
- 2-Cyanoaniline
- 2-Cyanophenylamine
- Akos 91125
- Anthranilic Acid Nitrile
- Anthranilonitril
- Antranilonitrilo
- Benzonitrile, 2-amino-
- O-Aminobenzonitrile
- O-Cyanoaniline
- Anthranilonitrile
- 2-Aminobenzontrile
- 2-Aminoobenzonitrile
- Aminobenzonitrile
- Anthranilonitrile~2-Cyanoaniline
- LABOTEST-BB LTBB000570
- 2-Aminobenzonitrile, (Anthranilonitrile
- AMINOBENZONITRILE(2-)
- 2-AMINO BENZONITRILE (2-CYANO ANILINE)
- Benzonitrile, o-amino-
- See more synonyms
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Found 9 products.
2-Aminobenzonitrile, 98%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C7H6N2Purity:98%Color and Shape:Crystalline powder, flakes, prills or chunks, White to cream or pale yellow/yellow to pale brownMolecular weight:118.14Ref: IN-DA002GXR
1g20.00€5g22.00€10g26.00€25g27.00€50g44.00€5kgTo inquire100g60.00€10kgTo inquire25kgTo inquire500g167.00€2-Aminobenzonitrile
CAS:<p>2-Aminobenzonitrile</p>Formula:C7H6N2Purity:98%Color and Shape: off-white solidMolecular weight:118.14g/mol2-Aminobenzonitrile
CAS:<p>2-Aminobenzonitrile is an aromatic amine and nitrile compound widely used in biochemical experiments and drug synthesis research.</p>Formula:C7H6N2Purity:99.73%Color and Shape:SolidMolecular weight:118.142-Aminobenzonitrile
CAS:Formula:C7H6N2Purity:>98.0%(GC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:118.142-Aminobenzonitrile
CAS:<p>2-Aminobenzonitrile is an organic compound with the chemical formula C6H5CN. It is a colorless liquid that is soluble in water and polar solvents. 2-Aminobenzonitrile can be synthesized by the reaction of ethylene diamine with phosphorus pentoxide, which yields 2-aminobenzonitrile and hydrogen cyanide as products. The uv absorption spectrum of 2-aminobenzonitrile exhibits maxima at 220 nm and 240 nm, indicating the presence of a cyano group. This cyano group reacts with malonic acid to form a Schiff base, which can then react with hydrogen to produce an intramolecular hydrogen bond between the two amine groups. Hydrogen chloride or trifluoroacetic acid can be used to deprotonate the amine groups on either side of the Schiff base, resulting in cleavage of the hydrogen bond and formation of benzene rings on each</p>Formula:C7H6N2Color and Shape:PowderMolecular weight:118.14 g/mol2-Aminobenzonitrile
CAS:Controlled Product<p>Applications Used for induction of nitrilase activity in Arthrobacter. Used as radioprotective agent.<br>References Houseman, A., et al.: Biochem. 32, 4430 (1993),<br></p>Formula:C7H6N2Color and Shape:NeatMolecular weight:118.14








