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61652-82-2

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61652-82-2 Usage

Molecular weight

193.17 g/mol

Chemical family

Imidazole

Usage

Building block in the synthesis of pharmaceuticals and agrochemical products

Potential properties

Antifungal and antitumor

Value in research

Valuable compound in medicinal chemistry research

Other applications

Reagent in organic synthesis, intermediate in production of dyes and pigments

Check Digit Verification of cas no

The CAS Registry Mumber 61652-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,5 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61652-82:
(7*6)+(6*1)+(5*6)+(4*5)+(3*2)+(2*8)+(1*2)=122
122 % 10 = 2
So 61652-82-2 is a valid CAS Registry Number.

61652-82-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name imidazol-1-yl-(3-nitrophenyl)methanone

1.2 Other means of identification

Product number -
Other names m-nitrobenzoylimidazole

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:61652-82-2 SDS

61652-82-2Relevant articles and documents

Synthesis of Dithiolethiones and Identification of Potential Neuroprotective Agents via Activation of Nrf2-Driven Antioxidant Enzymes

Bai, Feifei,Fang, Jianguo,Song, Zi-Long,Zhang, Baoxin

, p. 2214 - 2231 (2020/03/06)

Oxidative stress is implicated in the pathogenesis of a wide variety of neurodegenerative disorders, and accordingly, dietary supplement of exogenous antioxidants or/and upregulation of the endogenous antioxidant defense system are promising for therapeutic intervention or chemoprevention of neurodegenerative diseases. Nrf2, a master regulator of the cellular antioxidant machinery, cardinally participates in the transcription of cytoprotective genes against oxidative/electrophilic stresses. Herein, we report the synthesis of 59 structurally diverse dithiolethiones and evaluation of their neuroprotection against 6-hydroxydopamine-or H2O2-induced oxidative damages in PC12 cells, a neuron-like rat pheochromocytoma cell line. Initial screening identified compounds 10 and 11 having low cytotoxicity but conferring remarkable protection on PC12 cells from oxidative-mediated damages. Further studies demonstrated that both compounds upregulated a battery of antioxidant genes as well as corresponding genes' products. Significantly, silence of Nrf2 expression abolishes cytoprotection of 10 and 11, indicating targeting Nrf2 activation is pivotal for their cellular functions. Taken together, the two lead compounds discovered here with potent neuroprotective functions against oxidative stress via Nrf2 activation merit further development as therapeutic or chemopreventive candidates for neurodegenerative disorders.

Imidazole-1-yl pyrimidine derivatives, or pharmacutically acceptable salt thereof, and pharmaceutic composition comprising the same as an active ingredient

-

Page/Page column 15, (2016/08/17)

The present invention relates to a novel imidazole-1-yl pyrimidine derivative, a pharmaceutically acceptable salt thereof, and a pharmaceutic composition comprising the same. Since the imidazole-1-yl pyrimidine derivative according to the present inventio

One-pot Synthesis of β-Keto Sulfones and β-Keto Sulfoxides from Carboxylic Acids

Ibarra, C. Alvarez,Rodriguez, R. Cuervo,Monreal, M. C. Fernandez,Navarro, F. J. Garcia,Tesorero, J. Martin

, p. 5620 - 5623 (2007/10/02)

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