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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)-

Benzonitrile, 2,5-diamino-

N#Cc1cc(N)ccc1N Request for Quotation
Chemical Name: Benzonitrile, 2,5-diamino-
CAS Number: 14346-13-5
Product Number: AG009AD0(AGN-PC-00NJ1I)
Synonyms:
MDL No:
Molecular Formula: C7H7N3
Molecular Weight: 133.1506

Identification/Properties

Computed Properties
Molecular Weight:
133.154g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
133.064g/mol
Monoisotopic Mass:
133.064g/mol
Topological Polar Surface Area:
75.8A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
158
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,5-Diaminobenzonitrile is a versatile chemical compound widely used in chemical synthesis as a building block for various organic reactions. This compound plays a crucial role in the pharmaceutical industry as a key intermediate in the synthesis of biologically active molecules. Its unique chemical structure enables it to participate in a variety of reactions, such as nucleophilic substitution, condensation, and cyclization reactions.In organic synthesis, 2,5-Diaminobenzonitrile can be used to synthesize heterocyclic compounds, which are essential in drug discovery and development. By reacting with different reagents and functional groups, it can form complex structures that possess specific biological activities. Additionally, its ability to act as a nucleophile makes it a valuable reagent in the formation of carbon-carbon and carbon-nitrogen bonds, further expanding its synthetic utility.Moreover, 2,5-Diaminobenzonitrile can serve as a starting material for the preparation of fluorescent dyes, polymers, and other specialty chemicals. Its role in chemical synthesis extends to the fields of materials science, catalysis, and organic electronics. Overall, the versatile applications of 2,5-Diaminobenzonitrile make it a valuable compound in the realm of chemical synthesis and organic chemistry.