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4-bromo-N-(4-fluorophenyl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

346723-41-9

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346723-41-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 346723-41-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,6,7,2 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 346723-41:
(8*3)+(7*4)+(6*6)+(5*7)+(4*2)+(3*3)+(2*4)+(1*1)=149
149 % 10 = 9
So 346723-41-9 is a valid CAS Registry Number.

346723-41-9 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Alfa Aesar

  • (H57409)  4-Bromo-N-(4-fluorophenyl)benzamide, 97%   

  • 346723-41-9

  • 250mg

  • 1470.0CNY

  • Detail
  • Alfa Aesar

  • (H57409)  4-Bromo-N-(4-fluorophenyl)benzamide, 97%   

  • 346723-41-9

  • 1g

  • 4704.0CNY

  • Detail

346723-41-9Relevant academic research and scientific papers

Derivatives with uracil-benzothiazole structure, preparation method of derivatives, and application of anti-HCV drugs

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Paragraph 0061-0063, (2019/12/02)

According to the invention, a new series of uracil-benzothiazole NS5B RdRp inhibitors are designed and synthesized; the compounds have the structure shown in a general formula (1), wherein the uracil-benzothiazole NS5B RdRp inhibitor provided by the inven

ANTIMYCOTIC TRIAZOLE COMPOUND

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Page/Page column 4; 15, (2017/07/08)

The invention relates to Compound (I), which is 4-(4-(4-(((3R,5R)-5-((1H-1,2,4-triazol-1-yl)methyl)-5-(2,4-difluorophenyl)tetrahydrofuran-3-yl)methoxy)phenyl)piperazin-1-yl)-N-(4-fluorophenyl)benzamide, or a pharmaceutically acceptable salt thereof, usefu

ANTIMYCOTIC COMPOUND

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Page/Page column 20-21, (2016/06/28)

This invention relates to a compound, as defined in the specification, useful in the treatment of mycoses, compositions containing it and its use in therapy.

Hypervalent iodine mediated para -selective fluorination of anilides

Tian, Tian,Zhong, Wen-He,Meng, Shuai,Meng, Xiang-Bao,Li, Zhong-Jun

, p. 728 - 732 (2013/02/25)

A metal-free method for the direct regioselective fluorination of anilides has been developed. In the presence of bis(tert-butylcarbonyloxy)iodobenzene (PhI(OPiv)2) and hydrogen fluoride-pyridine, the para-fluorination products of anilides were obtained in moderate to good yields. Because of its operational safety and the use of readily available reagents, this new procedure provides facile access to a variety of para-fluorinated anilides.

Role of Hetero-halogen (F · · · X, X = Cl, Br, and I) or homo-halogen (X · · · X, X = F, Cl, Br, and I) interactions in substituted benzanilides

Nayak, Susanta K.,Kishore Reddy,Row, Tayur N. Guru,Chopra, Deepak

experimental part, p. 1578 - 1596 (2012/04/04)

A series of halogen-substituted benzanilides have been synthesized and characterized, and crystallization studies directed toward generation of polymorphs have been performed to delineate the importance of interactions involving halogens. The effect of ha

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