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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-Naphthalenemethanol, a-methyl-, (aS)-

C[C@@H](c1ccc2c(c1)cccc2)O Request for Quotation
Chemical Name: 2-Naphthalenemethanol, a-methyl-, (aS)-
CAS Number: 27544-18-9
Product Number: AG003CE2(AGN-PC-0R3CKR)
Synonyms:
MDL No:
Molecular Formula: C12H12O
Molecular Weight: 172.2231

Identification/Properties

Properties
MP:
70-71 °C
Storage:
Room Temperature;
Form:
Solid
Refractive Index:
-38 ° (C=1, MeOH)
Computed Properties
Molecular Weight:
172.227g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
172.089g/mol
Monoisotopic Mass:
172.089g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
167
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#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-1-(Naphthalen-2-yl)ethanol, also known as (S)-2-naphthylethanol, is a valuable compound widely used in chemical synthesis due to its unique properties and versatile reactivity. In organic chemistry, this chiral alcohol serves as a key building block for the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Its stereochemistry plays a crucial role in asymmetric synthesis, enabling the creation of enantiomerically pure compounds with high selectivity and efficiency.One common application of (S)-1-(Naphthalen-2-yl)ethanol is in the synthesis of chiral ligands and catalysts for asymmetric transformations. By utilizing this compound as a starting material, chemists can introduce a chiral center into their target molecules, leading to the formation of products with specific stereochemical arrangements. This is particularly important in the pharmaceutical industry, where the biological activity of drugs often depends on their stereochemistry.Furthermore, (S)-1-(Naphthalen-2-yl)ethanol can be employed in the synthesis of complex natural products and natural product derivatives. Its unique structural features and reactivity make it a valuable intermediate for the construction of diverse chemical scaffolds found in bioactive compounds. By incorporating this chiral alcohol into multi-step synthetic pathways, chemists can access a wide range of structurally and stereochemically diverse molecules with potential applications in drug discovery and development.Overall, the application of (S)-1-(Naphthalen-2-yl)ethanol in chemical synthesis highlights its importance as a versatile building block for the construction of complex molecules with specific stereochemical properties. Its role in asymmetric synthesis, ligand/catalyst design, and natural product synthesis underscores its significance in modern organic chemistry research and development.