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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-Undecanol

CCCCCC(CCCCC)O Request for Quotation
Chemical Name: 6-Undecanol
CAS Number: 23708-56-7
Product Number: AG0034DN(AGN-PC-0JKMA7)
Synonyms:
MDL No:
Molecular Formula: C11H24O
Molecular Weight: 172.3077

Identification/Properties

Properties
MP:
25-26°C
BP:
229.7°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Refractive Index:
1.4374
Computed Properties
Molecular Weight:
172.312g/mol
XLogP3:
4.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
8
Exact Mass:
172.183g/mol
Monoisotopic Mass:
172.183g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
71.1
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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:
Signal Word:
Danger
UN#:
1325
Hazard Statements:
H228
Precautionary Statements:
P210-P240-P241-P280
Class:
4.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Undecanol, a long-chain primary alcohol, is a versatile compound commonly used in various chemical synthesis processes. In organic chemistry, 6-Undecanol serves as a valuable starting material for the synthesis of fragrances, flavors, and pharmaceutical compounds. Its unique structure and reactivity make it an ideal building block for creating a wide range of organic molecules.Due to its long carbon chain, 6-Undecanol can be easily functionalized to introduce different functional groups, allowing chemists to tailor the properties of the final products. This compound is often employed in the synthesis of esters, ethers, and other derivatives through various chemical reactions such as esterification, oxidation, and reduction.Furthermore, 6-Undecanol can also be utilized as a solvent or a surfactant in chemical processes. Its amphiphilic nature enables it to interact with both polar and nonpolar compounds, making it an effective emulsifier in formulations such as cosmetics and personal care products.Overall, 6-Undecanol plays a crucial role in chemical synthesis, offering multiple avenues for the creation of complex organic compounds and enhancing the diversity of chemical transformations in the laboratory.