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2-(trifluoromethyl)-7-quinolinol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41192-81-8

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41192-81-8 Usage

Also known as

CF3Q

Type of compound

Fluorinated derivative of 7-quinolinol

Structural feature

Trifluoromethyl group attached to the second position of the quinolinol ring

Classification

Fluorinated arene

Uses

Ligand in organometallic chemistry, building block in the synthesis of pharmaceuticals and agrochemicals

Potential applications

Catalysis and material science

Unique properties

Structural and electronic properties

Check Digit Verification of cas no

The CAS Registry Mumber 41192-81-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,1,9 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 41192-81:
(7*4)+(6*1)+(5*1)+(4*9)+(3*2)+(2*8)+(1*1)=98
98 % 10 = 8
So 41192-81-8 is a valid CAS Registry Number.

41192-81-8Downstream Products

41192-81-8Relevant academic research and scientific papers

Tetracyclic pyrimidinone compound, preparation method, composition and application thereof

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Paragraph 0242-0243; 0247-0249, (2021/03/31)

A tetracyclic pyrimidinone compound represented by a formula (I) or a pharmaceutically acceptable salt thereof has a structure represented by a formula (I), is a brand new Lp-PLA2 inhibitor, and can be used for treating neurodegenerative related diseases such as Alzheimer's disease (AD), glaucoma, age-related macular degeneration (AMD), or cardiovascular diseases including atherosclerosis and thelike.

3-Trifloxy-3-trifluoromethylpropeniminium triflate: Reaction with aromatic amines - An efficient synthesis of 2-trifluoromethylquinolines

Baraznenok, Ivan L.,Nenajdenko, Valentine G.,Balenkova, Elizabeth S.

, p. 937 - 941 (2007/10/03)

The reaction of iminium triflates 2 and 7 with various aromatic amines were investigated. The 2-R(f)-substituted quinolines 3 and 8 were prepared in excellent yields by the reaction of 2 and 7, respectively, with substituted anilines. The reactions of 2 a

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