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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-Propen-1-ol, 3-(2-pyridinyl)-, (E)-

OC/C=C/c1ccccn1 Request for Quotation
Chemical Name: 2-Propen-1-ol, 3-(2-pyridinyl)-, (E)-
CAS Number: 113985-52-7
Product Number: AG003C0E(AGN-PC-0NYCH4)
Synonyms:
MDL No:
Molecular Formula: C8H9NO
Molecular Weight: 135.1632

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Chemical Structure


With its unique chemical structure, (E)-3-(Pyridin-2-yl)prop-2-en-1-ol serves as a valuable reagent in organic synthesis. This compound is commonly utilized for its ability to participate in various reactions, particularly in the formation of new carbon-carbon or carbon-heteroatom bonds. In chemical synthesis, (E)-3-(Pyridin-2-yl)prop-2-en-1-ol can act as a versatile building block for the construction of complex molecules. Its presence can enable the introduction of functional groups or modification of existing functionalities in target compounds. Overall, the application of (E)-3-(Pyridin-2-yl)prop-2-en-1-ol in chemical synthesis showcases its significance in expanding the scope of organic transformations and facilitating the creation of diverse molecular structures.