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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 articles and documents

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.

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