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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)-

1,2-Octanediol, (2R)-

CCCCCC[C@H](CO)O Request for Quotation
Chemical Name: 1,2-Octanediol, (2R)-
CAS Number: 87720-90-9
Product Number: AG004GH2(AGN-PC-0OL87U)
Synonyms:
MDL No:
Molecular Formula: C8H18O2
Molecular Weight: 146.2273

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Chemical Structure


In chemical synthesis, 1,2-Octanediol, (2R)- is a valuable compound that serves as a versatile building block for creating various chemical substances. Due to its unique structure and reactivity, this compound is commonly used as a precursor in the synthesis of a wide range of organic molecules. Its primary function lies in its ability to act as a diol, with two hydroxyl groups positioned on adjacent carbon atoms. This structural feature makes 1,2-Octanediol, (2R)- a key intermediate in the formation of polyesters, polyurethanes, and other polymers. Additionally, it can participate in reactions such as esterification, etherification, and oxidation to yield products with diverse functionalities. Its role in chemical synthesis extends to the production of pharmaceuticals, fragrances, and various specialty chemicals, highlighting its significance in the field of organic chemistry.