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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)-

2-pyridin-4-ylacetonitrile;hydrochloride

N#CCc1ccncc1.Cl Request for Quotation
Chemical Name: 2-pyridin-4-ylacetonitrile;hydrochloride
CAS Number: 92333-25-0
Product Number: AG003M0O(AGN-PC-0NIWEP)
Synonyms:
MDL No:
Molecular Formula: C7H7ClN2
Molecular Weight: 154.5969

Identification/Properties

Properties
MP:
267 °C
BP:
254.24°C (rough estimate)
Storage:
2-8℃;
Form:
Solid
Refractive Index:
1.5500 (estimate)
Computed Properties
Molecular Weight:
154.597g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
154.03g/mol
Monoisotopic Mass:
154.03g/mol
Topological Polar Surface Area:
36.7A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
116
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302+H312+H332-H315-H319-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Pyridineacetonitrile hydrochloride (1:1) is a versatile compound commonly used in chemical synthesis as a key intermediate in the production of pharmaceuticals, agrochemicals, and fine chemicals. This compound serves as a valuable building block in organic synthesis, particularly in the formation of heterocyclic compounds due to the presence of the pyridine ring structure. Its ability to undergo various chemical transformations, such as substitution reactions and condensations, allows for the creation of complex and diverse molecular structures. Additionally, the hydrochloride salt form enhances solubility and stability, making it particularly useful in reactions that require an aqueous environment.