CAS 25501-32-0

S(+)-1-indanol

Description:

S(+)-1-indanol, with the CAS number 25501-32-0, is a chiral organic compound that belongs to the class of indanols, which are derivatives of indane. This compound features a hydroxyl group (-OH) attached to the indane structure, specifically at the 1-position, contributing to its unique properties. S(+)-1-indanol is characterized by its optically active nature, meaning it can rotate plane-polarized light due to its chiral center. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. The compound is soluble in organic solvents and has limited solubility in water. S(+)-1-indanol is of interest in various fields, including pharmaceuticals and organic synthesis, due to its potential applications in the development of chiral catalysts and intermediates. Its stereochemistry plays a crucial role in its reactivity and interactions in biological systems, making it a valuable compound for research in asymmetric synthesis and medicinal chemistry.

Formula: C₉H₁₀O

InChI: InChI=1/C9H10O/c10-9-6-5-7-3-1-2-4-8(7)9/h1-4,9-10H,5-6H2/t9-/m0/s1

SMILES: c1ccc2c(c1)CC[C@@H]2O

Synonyms:

• (S)-(+)-1-Hydroxyindan
• (1S)-2,3-Dihydro-1H-indene-1β-ol
• (1S)-Indan-1β-ol
• (3S)-Indan-3-ol
• (S)-2,3-Dihydro-1H-indene-1β-ol
• [1S,(+)]-1-Indanol
• (1S)-2,3-dihydro-1H-inden-1-ol
• (S)-(+)-1-Indanol

(S)-2,3-Dihydro-1H-inden-1-ol

CAS: 25501-32-0

Formula: C₉H₁₀O

Purity: 97%

Color and Shape: Solid

Molecular weight: 134.1751

Ref: IN-DA0032FW

(S)-2,3-Dihydro-1H-inden-1-ol

CAS: 25501-32-0

(S)-2,3-Dihydro-1H-inden-1-ol

Purity: 97%

Molecular weight: 134.18g/mol

Ref: 54-OR510195

(S)-(+)-1-Indanol

CAS: 25501-32-0

Formula: C₉H₁₀O

Molecular weight: 134.18

Ref: 7W-GL9370

(S)-(+)-1-Indanol

CAS: 25501-32-0

(S)-(+)-1-Indanol is a substrate for the human liver alcohol dehydrogenase and can be used to study the enzyme. The molecule has two phenyl groups that are capable of forming hydrogen bonds with other molecules. The hydrogen bond is a relatively weak, noncovalent interaction between two polar molecules. It can be formed by the donation of a lone pair of electrons from one side of an oxygen atom in one molecule to a lone pair of electrons on another oxygen atom in another molecule. This type of bond is responsible for many important biological processes, including DNA replication and protein folding. The (S)-(+)-1-Indanol can also undergo carbonyl reduction, which is the conversion of an organic compound containing a carbonyl group into a corresponding hydrocarbon derivative containing hydroxyl groups. The (S)-(+)-1-Indanol contains both hydroxyl and carbonyl functionalities that make it suitable for this process. (S)-

Formula: C₉H₁₀O

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 134.18 g/mol

Ref: 3D-FI41787

(S)-2,3-Dihydro-1H-inden-1-ol

CAS: 25501-32-0

Purity: 97%

Molecular weight: 134.1779938

Ref: 10-F791262