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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Propanenitrile, 3-[(2-chlorophenyl)amino]-

N#CCCNc1ccccc1Cl Request for Quotation
Chemical Name: Propanenitrile, 3-[(2-chlorophenyl)amino]-
CAS Number: 94-89-3
Product Number: AG006QW0(AGN-PC-0JL7DI)
Synonyms:
MDL No:
Molecular Formula: C9H9ClN2
Molecular Weight: 180.6342

Identification/Properties

Properties
BP:
358.4 °C at 760 mmHg

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H312-H332
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 3-[(2-Chlorophenyl)amino]propanenitrile holds great importance in chemical synthesis as a versatile building block. Its unique structure allows it to participate in a variety of organic reactions, making it a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. 1. **Substitution Reactions**: The presence of the chloro group on the phenyl ring enables 3-[(2-Chlorophenyl)amino]propanenitrile to undergo nucleophilic aromatic substitution reactions. This property is particularly useful in introducing functional groups at specific positions on aromatic rings in the target molecules.2. **Amidation Reactions**: The amino group in the molecule can participate in amidation reactions, allowing for the formation of amide linkages with carboxylic acids. This functionality is crucial in the synthesis of peptides, pharmaceuticals, and other bioactive compounds.3. **Nitrile Group Reactions**: The nitrile group in 3-[(2-Chlorophenyl)amino]propanenitrile can undergo various transformations such as hydrolysis to carboxylic acids, reduction to primary amines, or conversion to other functional groups. This flexibility makes it a key component in the construction of complex molecular structures.Overall, the diverse reactivity and functional groups present in 3-[(2-Chlorophenyl)amino]propanenitrile make it an essential building block for chemists engaged in the synthesis of valuable compounds across different industries.