772-28-1

Basic information

• Product Name: 1H-Indene-2-ethanol, 2,3-dihydro-
• Synonyms: 1H-Indene-2-ethanol, 2,3-dihydro-;2-(2,3-dihydro-1H-inden-2-yl)ethanol
• CAS NO: 772-28-1
• Molecular Formula: C₁₁H₁₄O
• Molecular Weight: 162.23
• Mol File: 772-28-1.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H-Indene-2-ethanol, 2,3-dihydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indene-2-ethanol, 2,3-dihydro-(772-28-1)
• EPA Substance Registry System: 1H-Indene-2-ethanol, 2,3-dihydro-(772-28-1)

Safety Data

• Hazardous Substances Data: 772-28-1(Hazardous Substances Data)

Usage

Also known as

2,3-dihydro-1H-indene-2-ethanol

Physical state

Colorless liquid

Odor

Floral and woody

Usage

Production of flavors and fragrances

Additional use

Solvent for various applications

Application

Synthesis of other organic compounds

Health hazards

Potential health hazards

Precautions

Take necessary safety measures when handling and using the compound

Upstream product

• 615-13-4 2-indanone 
• 66658-02-4 acetic acid, (1,3-dihydro-2H-inden-2-ylidene)-, methyl ester 
• 157406-12-7 (E)-2-(1-oxo-1,3-dihydro-2H-inden-2-ylidene)acetic acid 
• 7664-93-9 sulfuric acid 
• 37868-26-1 2-(indan-2-yl)acetic acid 
• 53273-37-3 indan-2-yl-acetic acid methyl ester 
• 114915-75-2 1-oxoindan-Δ^2,α-acetic acid 
• 83-33-0 inden-1-one 
• 143356-09-6 ethyl 2-indanylacetate 

Downstream Products

• 159011-42-4 1-bromo-2-(2-indanyl)ethane 

Relevant articles and documents

Multiple Halogenation of Aliphatic C?H Bonds within the Hofmann–L?ffler Manifold

An innovative approach to position-selective polyhalogenation of aliphatic hydrocarbon bonds is presented. The reaction proceeded within the Hofmann-L?ffler manifold with amidyl radicals as the sole mediators to induce selective 1,5- and 1,6-hydrogen-atom transfer followed by halogenation. Multiple halogenation events of up to four innate C?H bond functionalizations were accomplished. The broad applicability of this new entry into polyhalogenation and the resulting synthetic possibilities were demonstrated for a total of 27 different examples including mixed halogenations.

TRICYCLIC 1,2,4-TRIAZINE OXIDES AND COMPOSITIONS THEREFROM FOR THERAPEUTIC USE IN CANCER TREATMENTS

The invention relates to novel tricyclic 1,2,4-triazine-1-oxides and novel tricyclic 1,2,4-triazine-1,4-dioxides of formula: (I); and to related analogues, to their preparation, and to their use as hypoxia-selective drugs and radiosensitizers for cancer therapy, both alone or in combination with radiation and/or other anticancer drugs.

Synthesis and thromboxane A2 antagonistic activity activity of indane derivatives.

A new series of indane derivatives were prepared and evaluated for their thromboxane A2 (TXA2, 1) antagonistic activity. Among these compounds, 24a (Z-335) was found to be a potent TXA2 antagonist in oral administration.