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Flucarbril is a novel chemical compound that has been developed for potential therapeutic applications. It is characterized by its unique molecular structure, which allows it to interact with specific biological targets. The compound is still in the research and development phase, with ongoing studies to determine its efficacy and safety in treating various medical conditions. As research progresses, the properties and potential uses of Flucarbril may be further elucidated, offering new insights into its role in healthcare and pharmaceuticals.

2261-94-1

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2261-94-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2261-94-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,6 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2261-94:
(6*2)+(5*2)+(4*6)+(3*1)+(2*9)+(1*4)=71
71 % 10 = 1
So 2261-94-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H8F3NO/c1-15-9-4-3-8(11(12,13)14)6-7(9)2-5-10(15)16/h2-6H,1H3

2261-94-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-6-(trifluoromethyl)quinolin-2-one

1.2 Other means of identification

Product number -
Other names Flucarbril [INN]

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:2261-94-1 SDS

2261-94-1Upstream product

2261-94-1Downstream Products

2261-94-1Relevant academic research and scientific papers

Silver-Catalyzed Decarboxylative Radical Addition/Cyclization of Oxamic Acids with Alkenes towards Quinolin-2-ones

Jin, Chengan,He, Jing-Yao,Bai, Qi-Fan,Feng, Gaofeng

, p. 1517 - 1522 (2020/08/10)

An efficient silver-catalyzed tandem decarboxylative radical addition/cyclization of oxamic acids with alkenes has been developed. This method provides a novel and straightforward protocol toward a variety of 4-aryl-3,4-dihydroquinolin-2(1 H)-ones, 4-(α-c

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