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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)-

4-(2-methyl-4-nitro-5-propan-2-yloxyphenyl)pyridine

CC(Oc1cc(c2ccncc2)c(cc1[N+](=O)[O-])C)C Request for Quotation
Chemical Name: 4-(2-methyl-4-nitro-5-propan-2-yloxyphenyl)pyridine
CAS Number: 1032903-62-0
Product Number: AG00HA0Z(AGN-PC-0D3SVM)
Synonyms:
MDL No:
Molecular Formula: C15H16N2O3
Molecular Weight: 272.2991

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-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


Employing 4-(5-isopropoxy-2-methyl-4-nitrophenyl)pyridine in chemical synthesis provides a valuable tool for creating novel compounds with enhanced properties. This versatile molecule serves as a key building block in the development of pharmaceuticals, agrochemicals, and materials science. Its unique structure enables the formation of diverse chemical bonds, facilitating the synthesis of complex organic compounds. In addition, its distinct reactivity pattern makes it well-suited for use in asymmetric synthesis and catalysis, allowing for the enantioselective production of chiral molecules. Furthermore, the presence of the nitro and isopropoxy functional groups confers specific chemical properties that can be leveraged for designing new bioactive molecules or functional materials. Overall, the strategic incorporation of 4-(5-isopropoxy-2-methyl-4-nitrophenyl)pyridine in chemical reactions offers a promising avenue for expanding the chemical space and unlocking new applications in diverse fields of chemistry.