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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)-

Indane-5-carbonitrile

N#Cc1ccc2c(c1)CCC2 Request for Quotation
Chemical Name: Indane-5-carbonitrile
CAS Number: 69975-67-3
Product Number: AG00FASJ(AGN-PC-0WCBL5)
Synonyms:
MDL No: MFCD09991848
Molecular Formula: C10H9N
Molecular Weight: 143.1852

Identification/Properties

Computed Properties
Molecular Weight:
143.189g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
143.073g/mol
Monoisotopic Mass:
143.073g/mol
Topological Polar Surface Area:
23.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
188
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,3-Dihydro-1H-indene-5-carbonitrile is a versatile compound commonly used in chemical synthesis for the production of various organic molecules. Due to its unique structure and reactive properties, this compound serves as a valuable building block in the creation of pharmaceuticals, agrochemicals, and fine chemicals. In particular, 2,3-Dihydro-1H-indene-5-carbonitrile is often employed in the synthesis of heterocyclic compounds, which are essential components in many advanced materials and biologically active substances. Its ability to undergo diverse chemical reactions enables researchers and chemists to access a wide range of novel compounds with potential applications in drug discovery, material science, and other fields of chemistry. By incorporating 2,3-Dihydro-1H-indene-5-carbonitrile into chemical synthesis pathways, scientists can efficiently generate complex molecules with tailored properties, paving the way for innovative advancements in various industries.