1. Home
  2. Tricyclo[3.3.1.13,7]decan-2-ol, 2-ethyl-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

Tricyclo[3.3.1.13,7]decan-2-ol, 2-ethyl-

CCC1(O)C2CC3CC1CC(C2)C3 Request for Quotation
Chemical Name: Tricyclo[3.3.1.13,7]decan-2-ol, 2-ethyl-
CAS Number: 14648-57-8
Product Number: AG001E2K(AGN-PC-0LAI28)
Synonyms:
MDL No:
Molecular Formula: C12H20O
Molecular Weight: 180.2866

Identification/Properties

Properties
MP:
70 °C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
180.291g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
180.151g/mol
Monoisotopic Mass:
180.151g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
193
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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2-Ethyladamantan-2-ol, also known as exo-2-ethyltricyclo[3.3.1.1^3,7]decane-2-ol, is a versatile compound commonly employed in chemical synthesis as a chiral building block. This unique molecule is characterized by its rigid and bulky structure, making it particularly useful in the development of pharmaceuticals and agrochemicals.One of the key applications of 2-Ethyladamantan-2-ol in chemical synthesis is its role as a chiral auxiliary in asymmetric synthesis. By utilizing this compound, chemists can introduce chirality into a molecule, enabling the production of enantiomerically pure compounds. This is crucial in the pharmaceutical industry, where the stereochemistry of a drug can significantly impact its efficacy and safety.Furthermore, 2-Ethyladamantan-2-ol can serve as a starting material for the synthesis of various complex organic molecules. Its unique structure provides a scaffold for building more elaborate structures through functional group transformations and carbon-carbon bond formations. This compound's steric hindrance also plays a crucial role in controlling regioselectivity and stereoselectivity in multi-step reactions.Overall, the application of 2-Ethyladamantan-2-ol in chemical synthesis showcases its significance as a valuable tool for accessing diverse and intricately designed molecules with high levels of stereochemical control.