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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)-

2-Hexanol, (2R)-

CCCC[C@H](O)C Request for Quotation
Chemical Name: 2-Hexanol, (2R)-
CAS Number: 26549-24-6
Product Number: AG002TNJ(AGN-PC-0O8FJ5)
Synonyms:
MDL No:
Molecular Formula: C6H14O
Molecular Weight: 102.1748

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
102.177g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
102.104g/mol
Monoisotopic Mass:
102.104g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
35.2
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


As a professional chemist, I can elaborate on the application of (R)-(-)-2-hexanol in chemical synthesis. With its chiral nature and specific structure, (R)-(-)-2-hexanol serves as a valuable building block in organic chemistry. It is commonly used as a versatile intermediate for the preparation of various compounds, including flavors, fragrances, and pharmaceuticals.In chemical synthesis, (R)-(-)-2-hexanol can participate in a range of reactions to introduce its unique stereochemical properties into the desired products. For instance, its alcohol functional group allows for diverse transformations, such as oxidation to form aldehydes or carboxylic acids, esterification to produce esters, or reduction to yield alcohols of different stereochemistry. Furthermore, the chiral nature of (R)-(-)-2-hexanol can influence the stereochemical outcomes of subsequent reactions, enabling the creation of enantiopure compounds crucial in medicinal chemistry and asymmetric catalysis.Overall, the versatility and stereochemical influence of (R)-(-)-2-hexanol make it a valuable tool in chemical synthesis, empowering chemists to access a wide array of complex molecules with precise stereochemistry for various applications in industry and research.