CAS 4254-29-9
:2-Indanol
Description:
2-Indanol, with the CAS number 4254-29-9, is an organic compound that belongs to the class of indanols, which are derivatives of indane. It features a hydroxyl (-OH) group attached to the second carbon of the indane structure, making it a secondary alcohol. This compound is typically a colorless to pale yellow liquid with a characteristic odor. 2-Indanol is known for its moderate solubility in water and good solubility in organic solvents, which is common for many alcohols. Its molecular formula is C9H10O, and it has a molecular weight that reflects its structure. The compound exhibits typical alcohol properties, such as the ability to participate in hydrogen bonding, which influences its boiling point and reactivity. 2-Indanol can be used in various applications, including as a solvent, in organic synthesis, and potentially in the fragrance industry due to its aromatic characteristics. Safety data indicates that it should be handled with care, as with many organic solvents, to avoid inhalation or skin contact.
Formula:C9H10O
InChI:InChI=1/C9H10O/c10-9-5-7-3-1-2-4-8(7)6-9/h1-4,9-10H,5-6H2
InChI key:InChIKey=KMGCKSAIIHOKCX-UHFFFAOYSA-N
SMILES:OC1CC=2C(C1)=CC=CC2
Synonyms:- 1H-Inden-2-ol, 2,3-dihydro-
- 2,3-dihydro-,1H-inden-2-ol
- 2-Hydroxyhydrindene
- 2-Hydroxyindan
- 2-Hydroxyindane
- Hydroxyindan,99%
- NSC 17485
- 2-Indanol
- indan-2-ol
- 2-lndanol
- 2-hydroxy-indane
- 2-Indanol,99%
- 2-INDANOL 99%
- See more synonyms
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Found 7 products.
2-Hydroxyindan
CAS:Formula:C9H10OPurity:>98.0%(GC)Color and Shape:White to Light yellow powder to crystalineMolecular weight:134.182-Hydroxyindane
CAS:<p>2-Hydroxyindane</p>Formula:C9H10OPurity:≥95%Color and Shape: light orange-brown solidMolecular weight:134.18g/mol2,3-Dihydro-1H-inden-2-ol
CAS:Formula:C9H10OPurity:95%Color and Shape:Crystalline PowderMolecular weight:134.1782-Indanol
CAS:<p>2-Indanol is a hydroxy compound that has a human immunodeficiency virus (HIV) replication inhibitor, antiviral activity, and structural formula. It has been shown to have anti-HIV activity in vitro at concentrations of 0.1 μM and 1 μM. 2-Indanol inhibits the process of reverse transcription by specifically binding to the hydroxyl group of the viral RNA polymerase and preventing it from making a hydrogen bond with the viral DNA template strand. 2-Indanol also slows down HIV replication by inhibiting protein synthesis. This inhibition is due to its ability to inhibit phosphorylation and dephosphorylation reactions in the host cell's ribosome machinery, which are required for protein synthesis. 2-Indanol has been shown to be active against covid-19 pandemic influenza viruses and has been used as an antiviral agent in mice infected with these viruses.</p>Formula:C9H10OPurity:Min. 95%Molecular weight:134.18 g/mol






