3199-77-7

Basic information

• Product Name: 2,3-DIHYDRO-5-METHOXY-1H-INDEN-1-OL
• Synonyms: 2,3-DIHYDRO-5-METHOXY-1H-INDEN-1-OL;5-methoxy-2,3-dihydro-1H-inden-1-ol;5-methoxyindan-1-ol;5-METHOXY-1-INDANOL
• CAS NO: 3199-77-7
• Molecular Formula: C₁₀H₁₂O₂
• Molecular Weight: 164.2
• Mol File: 3199-77-7.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 307.8°C at 760 mmHg
• Flash Point: 144.1°C
• Appearance: /
• Density: 1.176g/cm³
• Vapor Pressure: 0.000308mmHg at 25°C
• Refractive Index: 1.584
• CAS DataBase Reference: 2,3-DIHYDRO-5-METHOXY-1H-INDEN-1-OL(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-DIHYDRO-5-METHOXY-1H-INDEN-1-OL(3199-77-7)
• EPA Substance Registry System: 2,3-DIHYDRO-5-METHOXY-1H-INDEN-1-OL(3199-77-7)

Safety Data

• Hazardous Substances Data: 3199-77-7(Hazardous Substances Data)

Usage

General Description

2,3-Dihydro-5-methoxy-1H-inden-1-ol is a chemical compound with the molecular formula C10H12O2. It is a yellowish to brown liquid that is commonly used in the synthesis of various pharmaceuticals and organic compounds. 2,3-DIHYDRO-5-METHOXY-1H-INDEN-1-OL is also known for its distinct aromatic odor and is often used in the production of perfumes and fragrances. Additionally, 2,3-Dihydro-5-methoxy-1H-inden-1-ol has been studied for its potential medicinal properties, including its antibacterial and antifungal activities. Overall, this compound has a variety of industrial and research applications due to its unique chemical properties and potential biological activities.

InChI:InChI=1/C10H12O2/c1-12-8-3-4-9-7(6-8)2-5-10(9)11/h3-4,6,10-11H,2,5H2,1H3

Upstream product

• 5111-70-6 5-methoxy-1-indanone 
• 79827-88-6 5-methoxyindan-1-yl 3,5-dinitrobenzoate 
• 10516-71-9 3-(3-Methoxy-phenyl)-propionic acid 
• 1470-94-6 5-hydroxy-2,3-dihydro-1H-indene 
• 5111-69-3 5-methoxyindane 
• 38005-82-2 2,3-dihydro-1H-indene-1,5-diol 

Downstream Products

• 79827-88-6 5-methoxyindan-1-yl 3,5-dinitrobenzoate 
• 469904-27-6 5-methoxyindene 1,2-oxide 
• 753020-50-7 5-methoxy-trans-1,2-indandiol 
• 753020-50-7 5-methoxy-cis-1,2-indandiol 
• 1359938-25-2 C₂₁H₂₃NO 
• 1359938-26-3 C₂₈H₂₉NO 
• 1359938-27-4 C₂₁H₂₅NO 
• 1359938-28-5 C₂₈H₃₁NO 
• 5111-69-3 5-methoxyindane 
• 52372-95-9 2,3-dihydro-5-methoxy-1H-inden-1-amine 

Relevant articles and documents

PERIPHERAL ALKYL AND ALKENYL CHAINS EXTENDED BENZENE DERIVATIVES AND PHARMACEUTICAL COMPOSITION INCLUDING THE SAME

The compounds represented by Formula (I), which are peripheral alkyl and alkenyl chains extended benzene derivatives, are useful as dual autotaxin (ATX) / histone deacetylase (HD AC) inhibitors. These compounds may be included in a pharmaceutical composition along with a pharmaceutically acceptable carrier, and be used in a therapeutically effective amount for prophylaxis or treatment of various diseases and disorders.

Silylative Kinetic Resolution of Racemic 1-Indanol Derivatives Catalyzed by Chiral Guanidine

Efficient kinetic resolution of racemic 1-indanol derivatives was achieved using triphenylchlorosilane by asymmetric silylation in the presence of chiral guanidine catalysts. The chiral guanidine catalyst (R,R)-N-(1-(β-naphthyl)ethyl)benzoguanidine was found to be highly efficient as only 0.5 mol % catalyst loading was sufficient to catalyze the reaction of various substrates with appropriate conversion and high s-values (up to 89). This catalyst system was successfully applied to the gram-scale silylative kinetic resolution of racemic 1-indanol with high selectivity.

BICYCLICALLY SUBSTITUTED URACILS AND THE USE THEREOF

The present application relates to novel bicyclically substituted uracil derivatives, to processes for preparation thereof, to the use thereof alone or in combinations for treatment and/or prophylaxis of diseases, and to the use thereof for production of medicaments for treatment and/or prophylaxis of diseases.