CAS 1485-07-0
:2-naphthaleneethanol
Description:
2-Naphthaleneethanol, with the CAS number 1485-07-0, is an organic compound characterized by the presence of a naphthalene ring attached to an ethanol moiety. This compound typically appears as a white to off-white solid and is known for its aromatic properties due to the naphthalene structure. It is moderately soluble in organic solvents like ethanol and ether but has limited solubility in water. The compound exhibits both hydrophobic and hydrophilic characteristics, which can influence its behavior in various chemical environments. 2-Naphthaleneethanol can participate in various chemical reactions, including oxidation and esterification, making it useful in organic synthesis and as an intermediate in the production of other chemical compounds. Additionally, it may exhibit biological activity, which has led to investigations into its potential applications in pharmaceuticals and materials science. Safety data indicates that, like many aromatic compounds, it should be handled with care to avoid inhalation or skin contact, as it may pose health risks.
Formula:C12H12O
InChI:InChI=1/C12H12O/c13-8-7-10-5-6-11-3-1-2-4-12(11)9-10/h1-6,9,13H,7-8H2
InChI key:InChIKey=VCZANYLMPFRUHG-UHFFFAOYSA-N
SMILES:C(CO)C1=CC2=C(C=C1)C=CC=C2
Synonyms:- 2-(2-Hydroxyethyl)naphthalene
- 2-(2-Naphthalenyl)ethanol
- 2-(2-Naphthyl)ethanol
- 2-(2-Naphthyl)ethyl alcohol
- 2-(Naphthalen-2-Yl)Ethanol
- 2-(Naphthalen-2-yl)ethan-1-ol
- 2-Naphthalen-2-ylethanol
- 2-Naphthyl ethanol
- 2-β-Naphthylethanol
- NSC 21040
- Naphthalen-2-Ethanol
- 2-Naphthaleneethanol
- 2-NAPHTHALENE ETHANOL
- Naphthalene-2-ethanol
- See more synonyms
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Found 5 products.
2-(Naphthalen-2-yl)ethan-1-ol
CAS:<p>2-(Naphthalen-2-yl)ethan-1-ol</p>Purity:95%Molecular weight:172.22g/molNaphthalen-2-ethanol
CAS:<p>Naphthalen-2-ethanol is a primary alcohol that has been synthesized and immobilized onto boron nitride. It can be used as a synthetic reaction rate indicator. Naphthalen-2-ethanol is soluble in organic solvents such as methanol, which can be used to determine the concentration of methanol in solution by observing the change in absorbance at 230 nm. This compound has functional groups such as carbinols, which are characterized by their high reactivity and ability to form esters, ethers, amides, or nitriles. Naphthalen-2-ethanol also reacts with lipases to produce polyamines and with chromatography to produce substitutive nomenclature.</p>Formula:C12H12OPurity:Min. 95%Molecular weight:172.22 g/mol




