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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)-

4,7-Decadien-1-ol, (Z,Z)-

OCCC/C=C\C/C=C\CC Request for Quotation
Chemical Name: 4,7-Decadien-1-ol, (Z,Z)-
CAS Number: 104188-11-6
Product Number: AG00868P(AGN-PC-0NVP0R)
Synonyms:
MDL No:
Molecular Formula: C10H18O
Molecular Weight: 154.2493

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Chemical Structure


(4Z,7Z)-4,7-Decadien-1-ol, also known as dienol, is a versatile compound used extensively in chemical synthesis. Its unique double bond configuration makes it a valuable building block for creating various organic molecules. Specifically, in chemical synthesis, (4Z,7Z)-4,7-Decadien-1-ol serves as a key intermediate in the production of fragrances, flavors, and pharmaceuticals.Its conjugated diene structure allows for diverse reactions such as conjugate addition, hydrogenation, and cyclization, enabling the formation of complex molecular structures. Additionally, its hydroxyl group provides a site for further functionalization, allowing chemists to modify its properties for specific applications. Overall, (4Z,7Z)-4,7-Decadien-1-ol plays a crucial role in the synthesis of a wide range of compounds, making it an indispensable component in the toolkit of synthetic chemists.