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11H-indeno[1,2-b]quinolin-11-ol is a complex organic compound with the molecular formula C17H11NO. It belongs to the family of indenoquinolines, which are tricyclic aromatic compounds with a quinoline ring fused to an indene ring. This specific compound features a hydroxyl group (-OH) at the 11th position, which can participate in various chemical reactions, such as forming esters or ethers. It is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity. The compound's properties, such as solubility and stability, can be influenced by the presence of the hydroxyl group, making it an interesting target for further chemical exploration and potential drug development.

6626-65-9

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6626-65-9 Usage

Type of compound

Polycyclic aromatic compound

Structural components

Quinoline ring system
Benzene ring
Hydroxyl group

Potential applications

Pharmaceutical and medicinal

Unique structural properties

Facilitating its potential use in various applications

Exhibited properties

Antioxidant
Anti-inflammatory

Studied for

Potential anti-cancer effects
Neuroprotective effects

Ongoing research

Exploring its potential therapeutic applications

Check Digit Verification of cas no

The CAS Registry Mumber 6626-65-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6626-65:
(6*6)+(5*6)+(4*2)+(3*6)+(2*6)+(1*5)=109
109 % 10 = 9
So 6626-65-9 is a valid CAS Registry Number.

6626-65-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 11H-indeno[1,2-b]quinolin-11-ol

1.2 Other means of identification

Product number -
Other names 11H-indeno<1,2-b>quinolin-11-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6626-65-9 SDS

6626-65-9Downstream Products

6626-65-9Relevant academic research and scientific papers

Tandem radical reactions of isonitriles with 2-pyridonyl and other aryl radicals: Scope and limitations, and a first generation synthesis of (±)-camptothecin

Curran, Dennis P.,Liu, Hui,Josien, Hubert,Ko, Sung-Bo

, p. 11385 - 11404 (2007/10/03)

Photolysis of N-propargyl-6-halo-2-pyridones and related aromatic halides in the presence of aryl isonitriles provides tetra- and penta-cyclic products in a single step by a sequence of radical addition to the isonitrile followed by two cyclizations. The scope and limitations of the process are described along with a first generation synthesis of racemic camptothecin.

Carbocyclic and nitrogen-containing fused CH-acids with an annelated indenyl fragment. Thermogravimetric and X-ray structural analysis of 6H-indenoquinoline

Pleshakov, V. G.,Akimov, V. M.,Nava, E. Huipe,Lindeman, S. V.,Struchkov, Yu. T.,et al.

, p. 682 - 688 (2007/10/02)

Based on thermogravimetric characteristics first obtained for the model 6H-indenoquinoline, the scheme of thermal conversions of this compound in the temperature range 20-700 deg C has been proposed, and the limit of its thermal stability (ca. 300 deg C) has been determined.This temperature is recommended as the optimum for synthesizing fused benzoaza(diaza)fluorenes.Based on the results of X-ray structural analysis, the molecules of the studied indenoquinoline form centrosymmetric pairs, which are arranged in (110) layers.The molecules are orientationally disordered self-association of these molecules is similar to the ?-? association of fused heterocyclic systems with ?-excessive and ?-deficient fragments.It has been suggested that interferon-inducing and antitumor compounds with an annelated indenyl fragment have a common mechanism of action according to the intercalation model of stacking structures. - Key words: CH-acids; 6H-indenoquinoline, heterogeneous catalytic dehydrogenation, thermogravimetric and X-ray structural analysis; interferon-inducing and antitumor intercalators; topological factor; stacking structures.

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