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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)-

Cyclopropanecarboxylic acid, 1-(4-pyridinyl)-

OC(=O)C1(CC1)c1ccncc1 Request for Quotation
Chemical Name: Cyclopropanecarboxylic acid, 1-(4-pyridinyl)-
CAS Number: 920297-29-6
Product Number: AG00IH05(AGN-PC-0ALTAN)
Synonyms:
MDL No:
Molecular Formula: C9H9NO2
Molecular Weight: 163.1733

Identification/Properties

Computed Properties
Molecular Weight:
163.176g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
163.063g/mol
Monoisotopic Mass:
163.063g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
193
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(Pyridin-4-yl)cyclopropanecarboxylic acid is a versatile compound that finds wide application in chemical synthesis. As a key building block in organic chemistry, it serves as a crucial intermediate in the preparation of various functionalized cyclopropane derivatives. Due to the unique reactivity of the cyclopropane ring, this compound enables the introduction of structural diversity and complexity into organic molecules. Its distinct properties make it a valuable tool in the development of pharmaceuticals, agrochemicals, and materials science. By incorporating 1-(Pyridin-4-yl)cyclopropanecarboxylic acid into synthetic routes, chemists can access a diverse array of compounds with enhanced biological activity and physical properties.