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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)-

9-(2-Carboxy-2-cyanovinyl)julolidine

N#C/C(=Cc1cc2CCCN3c2c(c1)CCC3)/C(=O)O Request for Quotation
Chemical Name: 9-(2-Carboxy-2-cyanovinyl)julolidine
CAS Number: 142978-18-5
Product Number: AG009C15(AGN-PC-07CYMG)
Synonyms:
MDL No: MFCD00274408
Molecular Formula: C16H16N2O2
Molecular Weight: 268.3104

Identification/Properties

Computed Properties
Molecular Weight:
268.316g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
268.121g/mol
Monoisotopic Mass:
268.121g/mol
Topological Polar Surface Area:
64.3A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
456
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


9-(2-Carboxy-2-cyanovinyl)julolidine is a versatile compound widely used in chemical synthesis, particularly in the fields of organic chemistry and materials science. This compound serves as a key building block in the synthesis of fluorescent dyes and phosphorescent materials.In organic chemistry, 9-(2-Carboxy-2-cyanovinyl)julolidine is commonly employed as a fluorescent probe due to its unique optical properties. It can be used for labeling biomolecules in biological studies, such as tracking specific proteins or monitoring cellular processes. The compound's strong fluorescence emission makes it an ideal candidate for applications requiring sensitive detection methods.Moreover, in materials science, 9-(2-Carboxy-2-cyanovinyl)julolidine is utilized in the fabrication of organic light-emitting diodes (OLEDs) and other optoelectronic devices. Its ability to efficiently convert electrical energy into light, combined with its excellent stability and color tunability, makes it a valuable component in the development of advanced display technologies and lighting systems.Overall, the inclusion of 9-(2-Carboxy-2-cyanovinyl)julolidine in chemical synthesis processes enables the creation of innovative fluorescent materials and optoelectronic devices with enhanced performance characteristics, paving the way for exciting advancements in various fields of science and technology.