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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)-

1,13-Tetradecadiene

C=CCCCCCCCCCCC=C Request for Quotation
Chemical Name: 1,13-Tetradecadiene
CAS Number: 21964-49-8
Product Number: AG003D7J(AGN-PC-0JKLM0)
Synonyms:
MDL No:
Molecular Formula: C14H26
Molecular Weight: 194.35624

Identification/Properties

Computed Properties
Molecular Weight:
194.362g/mol
XLogP3:
6.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
11
Exact Mass:
194.203g/mol
Monoisotopic Mass:
194.203g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
108
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

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


1,13-Tetradecadiene, also known as tetradecadiene, is a compound widely utilized in chemical synthesis for its versatile applications. This organic compound consists of a chain of 14 carbon atoms with two double bonds strategically positioned at the 1st and 13th positions. Its unique molecular structure makes it a valuable building block in various synthesis processes.In organic chemistry, 1,13-tetradecadiene serves as a crucial intermediate in the production of polymers, resins, and other valuable chemicals. Its diene functionality allows it to participate in important reactions such as Diels-Alder cycloaddition, which enables the formation of complex ring structures. Additionally, its long carbon chain provides a platform for the introduction of functional groups and modifications, enhancing its utility in diverse chemical transformations.Moreover, 1,13-tetradecadiene finds extensive use in the synthesis of fragrances and flavors due to its ability to impart specific olfactory characteristics. By incorporating this compound into fragrance formulations, chemists can create unique scents that appeal to a wide range of preferences. Its role in flavor synthesis adds depth and complexity to food products, enhancing their overall sensory experience.Overall, 1,13-tetradecadiene plays a significant role in chemical synthesis across various industries, showcasing its importance as a versatile and multifunctional compound.