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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)-

6-Octen-1-ol, 3,7-dimethyl-, (3R)-

OCC[C@@H](CCC=C(C)C)C Request for Quotation
Chemical Name: 6-Octen-1-ol, 3,7-dimethyl-, (3R)-
CAS Number: 1117-61-9
Product Number: AG00HC6N(AGN-PC-0NXQSK)
Synonyms:
MDL No:
Molecular Formula: C10H20O
Molecular Weight: 156.2652

Identification/Properties

Computed Properties
Molecular Weight:
156.269g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
5
Exact Mass:
156.151g/mol
Monoisotopic Mass:
156.151g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
112
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

GHS Pictogram:
N/A
Signal Word:
UN#:
N/A
Hazard Statements:
-
Precautionary Statements:
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


A versatile and valuable molecule, (+)-Citronellol is often employed in chemical synthesis as a chiral building block. Its stereoselective reactivity makes it a particularly useful starting material for the synthesis of various fine chemicals and pharmaceuticals. Due to its unique structure and properties, (+)-Citronellol can undergo numerous chemical transformations such as oxidation, reduction, and functional group interconversion, allowing for the creation of complex and highly specific molecules. Its application in asymmetric synthesis enables the production of enantiomerically pure compounds, crucial in the pharmaceutical industry for enhancing drug efficacy and reducing side effects. Additionally, the ability of (+)-Citronellol to act as a precursor in the synthesis of fragrances, flavors, and bioactive compounds further highlights its significance in organic chemistry.