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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)-

1,6-Heptadien-4-ol, 4-(2-propenyl)-

C=CCC(CC=C)(CC=C)O Request for Quotation
Chemical Name: 1,6-Heptadien-4-ol, 4-(2-propenyl)-
CAS Number: 10202-75-2
Product Number: AG0006CC(AGN-PC-0JMQK9)
Synonyms:
MDL No:
Molecular Formula: C10H16O
Molecular Weight: 152.2334

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Chemical Structure


4-Allylhepta-1,6-dien-4-ol, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role in various organic reactions, primarily due to its unique allylic and dienic structure. One of the key applications of 4-Allylhepta-1,6-dien-4-ol in chemical synthesis is its involvement in Diels-Alder reactions. The diene functionality of this compound makes it an excellent dienophile in Diels-Alder cycloaddition reactions, allowing for the formation of complex cyclic structures with high regioselectivity and stereoselectivity. Additionally, 4-Allylhepta-1,6-dien-4-ol can serve as a valuable precursor for the synthesis of other functionalized molecules through various organic transformations such as allylation, oxidation, and reduction reactions. Its versatility and reactivity make it a valuable building block in the synthesis of natural products, pharmaceuticals, and fine chemicals.