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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)-

Pyridine, 4-[(1E)-2-phenylethenyl]-

c1ccc(cc1)C=Cc1ccncc1 Request for Quotation
Chemical Name: Pyridine, 4-[(1E)-2-phenylethenyl]-
CAS Number: 5097-93-8
Product Number: AG019LIA(AGN-PC-0OBFIG)
Synonyms:
MDL No:
Molecular Formula: C13H11N
Molecular Weight: 181.2331

Identification/Properties

Properties
MP:
128-132°C
Storage:
-10 ℃;Inert atmosphere;Light sensitive;
Form:
Solid
Computed Properties
Molecular Weight:
181.238g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
181.089g/mol
Monoisotopic Mass:
181.089g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
174
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
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


The compound 4-(2-Phenylvinyl)pyridine, trans- is a valuable reagent in chemical synthesis, specifically in the field of organic chemistry. Due to its unique structure and properties, this compound is commonly used as a key building block in the preparation of various organic molecules and pharmaceutical compounds. Its ability to undergo selective cross-coupling reactions makes it a versatile tool for the formation of complex molecular structures. Additionally, 4-(2-Phenylvinyl)pyridine, trans- is known to exhibit interesting biological activities, making it a promising candidate for medicinal chemistry research. In summary, this compound plays a crucial role in the development of novel synthetic routes and the discovery of biologically active compounds.