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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)-

3-(4-aminopyridin-2-yl)benzaldehyde;hydrochloride

O=Cc1cccc(c1)c1nccc(c1)N.Cl Request for Quotation
Chemical Name: 3-(4-aminopyridin-2-yl)benzaldehyde;hydrochloride
CAS Number: 1334500-04-7
Product Number: AG007NFD(AGN-PC-0BGIIG)
Synonyms:
MDL No:
Molecular Formula: C12H11ClN2O
Molecular Weight: 234.6815

Identification/Properties

Computed Properties
Molecular Weight:
234.683g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
234.056g/mol
Monoisotopic Mass:
234.056g/mol
Topological Polar Surface Area:
56A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
220
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The product 3-(4-Aminopyridin-2-yl)benzaldehyde hydrochloride is a versatile chemical compound widely utilized in various chemical synthesis processes. This compound serves as a key building block in the preparation of organic molecules and pharmaceutical intermediates. Its unique structure enables it to participate in a range of reactions, including condensation, oxidation, and reduction processes. In chemical synthesis, 3-(4-Aminopyridin-2-yl)benzaldehyde hydrochloride plays a crucial role in the production of heterocyclic compounds, dyes, and fine chemicals. Its ability to act as a functional group carrier and a catalyst in multiple reactions makes it an essential component in the synthesis of complex organic molecules with diverse applications in the pharmaceutical, agrochemical, and material science industries.