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N-(3-Fluorophenyl)-4-MethylbenzaMide, 97%, is a high-purity organic compound with the chemical formula C14H11FNO. It is a derivative of benzamide, featuring a 3-fluorophenyl group attached to the nitrogen atom and a methyl group on the 4-position of the benzene ring. N-(3-Fluorophenyl)-4-MethylbenzaMide, 97% is widely used in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structure and reactivity. The 97% purity indicates that the product contains a minimum of 97% of the desired compound, with the remaining 3% being other substances, which could be impurities or by-products from the synthesis process.

5215-30-5

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5215-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5215-30-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,1 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5215-30:
(6*5)+(5*2)+(4*1)+(3*5)+(2*3)+(1*0)=65
65 % 10 = 5
So 5215-30-5 is a valid CAS Registry Number.
InChI:InChI=1/C54H55N3O9/c1-3-26-64-54-50(57(53(60)38-17-14-35(32-55)15-18-38)33-36-16-22-48-49(27-36)63-34-62-48)31-46(56-61-2)44-29-40(12-6-8-24-58)43(13-7-9-25-59)51(52(44)54)45-30-42(21-23-47(45)66-54)65-41-20-19-37-10-4-5-11-39(37)28-41/h3-5,10-11,14-23,27-30,40,43,50-52,58-59H,1,6-9,12-13,24-26,31,33-34H2,2H3

5215-30-5Downstream Products

5215-30-5Relevant academic research and scientific papers

Direct amide synthesis: via Ni-mediated aminocarbonylation of arylboronic acids with CO and nitroarenes

Shen, Ni,Cheung, Chi Wai,Ma, Jun-An

supporting information, p. 13709 - 13712 (2019/11/19)

Herein we describe an alternative and unconventional approach of an aminocarbonylation reaction to access aryl amides from readily available and low-cost arylboronic acids and nitroarenes. Nickel metal can serve as both reductant and catalyst in this direct aminocarbonylation. This protocol exhibits a good functional group compatibility and allows a variety of aryl amides to be synthesized, including several drug-like molecules.

Antimycobacterial activity of 3'- and 4'-fluorothiobenzanilides

Waisser,Kunes,Odlerova,Roman,Kubicova,Horak

, p. 193 - 195 (2007/10/03)

On the basis of a preliminary study of the antimycobacterial activity of thiobenzanilides, a group of 3/-fluoro- and 4/fluorothiobenzanilides has been synthesized and tested against Mycobacterium tuberculosis, M. kansasii, M. avium and M. fortuitum. The r

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