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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-Octen-3-ol, (3S)-

CCCCC[C@@H](C=C)O Request for Quotation
Chemical Name: 1-Octen-3-ol, (3S)-
CAS Number: 24587-53-9
Product Number: AG002ONQ(AGN-PC-0O87B1)
Synonyms:
MDL No:
Molecular Formula: C8H16O
Molecular Weight: 128.2120

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Chemical Structure


(S)-1-Octen-3-ol, commonly known as octenol, is a versatile compound that finds extensive application in chemical synthesis. Its chiral nature, stemming from the presence of a stereocenter, makes it a valuable building block for the preparation of enantiopure compounds. In organic synthesis, (S)-1-Octen-3-ol serves as a key starting material for the production of various pharmaceuticals, flavors, and fragrances. Due to its distinct odor profile reminiscent of mushrooms, it is frequently used as a scent intermediate in the creation of perfumes and colognes. Additionally, its reactivity allows for the selective formation of different functionalized derivatives, thereby enabling the synthesis of a wide range of complex molecules with high stereochemical precision. This compound plays a crucial role in the development of novel chemical reactions and the advancement of synthetic methodologies in the field of organic chemistry.