215500-55-3 Usage
Chemical structure
1-(4-nitrophenyl)-5-(trifluoromethyl)-1H-pyrazole consists of a pyrazole ring with a 4-nitrophenyl group and a trifluoromethyl group attached to it.
Usage
It is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds.
Applications
NT1P has potential applications as a building block in drug discovery and development, as well as in materials science.
Safety
It is important to handle this chemical with caution and to use appropriate safety measures, as it may be hazardous if mishandled.
Chemical properties
The presence of the nitro group and the trifluoromethyl group in the molecule can influence its reactivity and stability.
Physical properties
The specific physical properties of NT1P, such as melting point, boiling point, and solubility, are not provided in the material.
Hazardous nature
The material suggests that NT1P may be hazardous if mishandled, but it does not provide specific information about its toxicity or potential health risks.
Regulatory status
The material does not provide information about the regulatory status of NT1P, such as whether it is classified as a hazardous substance or subject to specific handling or disposal requirements.
Environmental impact
The material does not provide information about the potential environmental impact of NT1P, such as its persistence in the environment or potential for bioaccumulation.
Check Digit Verification of cas no
The CAS Registry Mumber 215500-55-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,5,0 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 215500-55:
(8*2)+(7*1)+(6*5)+(5*5)+(4*0)+(3*0)+(2*5)+(1*5)=93
93 % 10 = 3
So 215500-55-3 is a valid CAS Registry Number.
215500-55-3Relevant academic research and scientific papers
A fluorine-containing oxazolidinone compounds and its preparation method and application
-
Paragraph 0040; 0042; 0088; 0090; 0091; 0092; 0093-0095, (2017/08/25)
The invention discloses a fluorine-containingoxazolidinonecompound as well as a preparation method and an application thereof. The structural formula of the fluorine-containingoxazolidinonecompound is as follows, wherein Rf refers to a trifluoromethyl group, a difluoromethyl group, a fluorine atom or perfluoralkane, R and Rindependently refer to H, C1-C6 straight-chain or branchedalkyl groups, C1-C6 straight-chain or branchedperfluoroalkyl groups, C1-C6 straight-chain or branchedalkoxygroups, a halogen such as F, Cl, Br or I, a nitro group, a cyano group or a phenyl group; R, R, R and Rindependently refer to H, F, Cl, Br, I or C1-C3 alkyl groups. The fluorine-containingoxazolidinonecompound has the better antimicrobial activity on watermelonanthracnose and cucumber grey mold and is particularly good in inhibitory activity on phytopathogencucumber grey mold of imperfect fungihyphomycetes, and a new choice is provided for development and utilization of new sterilization pesticides.
Synthesis and in vitro antibacterial activity of novel fluoroalkyl-substituted pyrazolyl oxazolidinones
Yan, Lili,Wu, Jingjing,Chen, Heng,Zhang, Shaowu,Wang, Zhi,Wang, Hui,Wu, Fanhong
, p. 73660 - 73669 (2015/09/15)
A series of novel oxazolidinone derivatives bearing fluoroalkyl-substituted pyrazole as the C-ring structure were designed, synthesized and evaluated for their antibacterial activity against six Gram-positive bacterial pathogens. Most of the target compounds have good antibacterial activity. Especially, compounds 13f, 13i and 13l show excellent activity comparable to linezolid.
