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2',4'-Difluoro-3-(4-methylpiperazine-1-carbonyl)biphenyl-4-yl benzoate is a synthetic chemical compound with potential pharmacological activity. It is a derivative of biphenyl-4-yl benzoate that has been modified to include a difluoro and a methylpiperazine-1-carbonyl moiety. 2',4'-Difluoro-3-(4-methylpiperazine-1-carbonyl)biphenyl-4-yl benzoate may exhibit biological activity through its interaction with specific cellular targets, and it may have applications in drug development and medicinal chemistry. However, further research is needed to fully understand the potential uses and effects of this chemical.

1095208-64-2

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1095208-64-2 Usage

Uses

Used in Drug Development:
2',4'-Difluoro-3-(4-methylpiperazine-1-carbonyl)biphenyl-4-yl benzoate is used as a potential pharmaceutical agent for its possible interaction with specific cellular targets. Its unique structure, which includes a difluoro and a methylpiperazine-1-carbonyl moiety, may contribute to its pharmacological properties, making it a candidate for further research and development in the field of medicinal chemistry.
Used in Medicinal Chemistry:
2',4'-Difluoro-3-(4-methylpiperazine-1-carbonyl)biphenyl-4-yl benzoate is used as a chemical entity in the exploration of new drug candidates. Its synthesis and modification may lead to the discovery of novel compounds with therapeutic potential, contributing to the advancement of medicinal chemistry and the development of new treatments for various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 1095208-64-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,5,2,0 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1095208-64:
(9*1)+(8*0)+(7*9)+(6*5)+(5*2)+(4*0)+(3*8)+(2*6)+(1*4)=152
152 % 10 = 2
So 1095208-64-2 is a valid CAS Registry Number.

1095208-64-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(2,4-difluorophenyl)-2-(4-methylpiperazine-1-carbonyl)phenyl] benzoate

1.2 Other means of identification

Product number -
Other names 2',4'-difluoro-3-(4-methylpiperazine-1-carbonyl)biphenyl-4-yl benzoate

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:1095208-64-2 SDS

1095208-64-2Downstream Products

1095208-64-2Relevant academic research and scientific papers

Synthesis and biological evaluation of amide derivatives of diflunisal as potential anti-inflammatory agents

Zhong, Guang-Xiang,Hu, Jin-Qing,Zhao, Kun,Chen, Lu-Lu,Hu, Wei-Xiao,Qiu, Ming-You

, p. 516 - 519 (2011/03/18)

To improve the medicinal activity, the structure of diflunisal has been modified. Twenty-one amide derivatives of diflunisal were synthesized starting from diflunisal in three steps with total yields from 72% to 89%. All compounds were identified by 1H NMR, MS, and elemental analysis. The anti-inflammatory and analgesic activities for 19 compounds were evaluated. It was found that 5m possesses an excellent anti-inflammatory activity and a good analgesic activity, maybe a potential anti-inflammatory agent.

Synthesis and biological evaluation of amide derivatives of diflunisal as potential anti-tumor agents

Zhong, Guang-Xiang,Chen, Lu-Lu,Li, Hai-Bo,Liu, Fu-Jin,Hu, Jin-Qing,Hu, Wei-Xiao

scheme or table, p. 4399 - 4402 (2010/04/05)

To discover the new medicinal activity, the structure of diflunisal has been modified. Forty amide derivatives of diflunisal were synthesized starting from diflunisal in three steps. Their inhibition growth rate of human lung cancer cell (A549) and human

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