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1-BENZYL-3-NITRO-1H-PYRAZOLE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

898053-27-5

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898053-27-5 Usage

Type of compound

Nitro-substituted pyrazole derivative

Usage

Synthesis of pharmaceuticals and agrochemicals

Nitro group

At the 3rd position on the pyrazole ring

Benzyl group

Attached to the nitrogen atom

Biological activities

Exhibits anti-inflammatory, antimicrobial, and antiviral properties

Reactivity

Presence of nitro group makes it a reactive compound

Safety precautions

Handle with caution in laboratory settings

Check Digit Verification of cas no

The CAS Registry Mumber 898053-27-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,0,5 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 898053-27:
(8*8)+(7*9)+(6*8)+(5*0)+(4*5)+(3*3)+(2*2)+(1*7)=215
215 % 10 = 5
So 898053-27-5 is a valid CAS Registry Number.

898053-27-5Downstream Products

898053-27-5Relevant academic research and scientific papers

Pyrazole N-alkylation method

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Paragraph 0033; 0034, (2018/12/14)

The invention provides a pyrazole N-alkylation method. Pyrazole or pyrazole derivatives and alkyl halogenated hydrocarbons react in a solvent under the existence of quaternary ammonium salt catalysts;N-alkyl substituted pyrazole is obtained. The method provided by the invention has the advantages that the operation is simple; the cost is low; the anhydrous oxygen-free environment is not needed; heating is not needed; the yield is high; the amplified industrialized production can be easily realized.

Regioselective Synthesis, NMR, and Crystallographic Analysis of N1-Substituted Pyrazoles

Huang, Adrian,Wo, Kellie,Lee, So Yeun Christine,Kneitschel, Nika,Chang, Jennifer,Zhu, Kathleen,Mello, Tatsiana,Bancroft, Laura,Norman, Natalie J.,Zheng, Shao-Liang

, p. 8864 - 8872 (2017/09/11)

A systematic study of the N-substitution reactions of 3-substituted pyrazoles under basic conditions has been undertaken. Regioselective N1-alkylation, -arylation, and -heteroarylation of 3-substituted pyrazoles have been achieved using K2CO3-DMSO. The regioselectivity is justified by the DFT calculations at the B3LYP/6-31G??(d) level. A consistent steric effect on chemical shift has been observed for N-alkyl pyrazole analogues. Twenty-five X-ray crystallographic structures have been obtained to confirm the regiochemistry of the major products.

SULFONYLUREAS AND RELATED COMPOUNDS AND USE OF SAME

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Page/Page column 136, (2016/09/15)

ABSTRACT The present invention provides for certain sulfonyl ureas and related compounds which have advantageous properties and show useful activity in the inhibition of activation of the NLRP3 inflammasome. Such compounds are useful in the treatment of a wide range of disorders in which the inflammation process, or more specifically the NLRP3 inflammasome, have been implicated as being a key factor.

Benzyl-1H-pyrazole and benzyl-1H-pyrazole derivatives, and preparation method and application thereof

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Paragraph 0069; 0070; 0071; 0072; 0085; 0086; 0087; 0088, (2016/10/09)

The invention belongs to the field of chemical medicine, and particularly relates to benzyl-1H-pyrazole and benzyl-1H-pyrazole derivatives, and a preparation method and application thereof. The structure of the benzyl-1H-pyrazole and benzyl-1H-pyrazole de

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