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BENZOPHENONE-2,4'-DICARBOXYLIC ACID is a chemical compound that belongs to the class of organic compounds known as benzoic acids and derivatives. It is characterized by the presence of two carboxylic acid functional groups in the 2 and 4' positions of the benzophenone structure. BENZOPHENONE-2,4'-DICARBOXYLIC ACID is typically a white crystalline powder at room temperature and exhibits aromatic, acidic properties. It is mainly utilized in scientific research and has potential applications in the manufacturing of various resins, pharmaceuticals, and polymers.

85-58-5

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85-58-5 Usage

Uses

Used in Scientific Research:
BENZOPHENONE-2,4'-DICARBOXYLIC ACID is used as a research chemical for studying its properties and potential applications in various fields.
Used in Resin Manufacturing:
BENZOPHENONE-2,4'-DICARBOXYLIC ACID is used as a chemical intermediate for the production of different types of resins, contributing to their structural and functional characteristics.
Used in Pharmaceutical Industry:
BENZOPHENONE-2,4'-DICARBOXYLIC ACID is used as a building block in the synthesis of pharmaceutical compounds, potentially leading to the development of new drugs.
Used in Polymer Production:
BENZOPHENONE-2,4'-DICARBOXYLIC ACID is used as a monomer or a component in the production of polymers, which can be utilized in various applications such as plastics, coatings, and adhesives.

Check Digit Verification of cas no

The CAS Registry Mumber 85-58-5 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 85-58:
(4*8)+(3*5)+(2*5)+(1*8)=65
65 % 10 = 5
So 85-58-5 is a valid CAS Registry Number.

85-58-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzophenone-2,4'-dicarboxylic Acid Monohydrate

1.2 Other means of identification

Product number -
Other names 2-(4-carboxybenzoyl)benzoic acid

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:85-58-5 SDS

85-58-5Relevant academic research and scientific papers

Synthesis, Cytotoxicity, and Mechanistic Investigation of Platinum(IV) Anticancer Complexes Conjugated with Poly(ADP-ribose) Polymerase Inhibitors

Xu, Zoufeng,Li, Cai,Zhou, Qiyuan,Deng, Zhiqin,Tong, Zixuan,Tse, Man-Kit,Zhu, Guangyu

, p. 16279 - 16291 (2019/11/28)

Many clinical trials using combinations of platinum drugs and PARP-1 inhibitors (PARPi) have been carried out, with the hope that such combinations will lead to enhanced therapeutic outcomes against tumors. Herein, we obtained seven potential PARPi with structural diversity and then conjugated them with cisplatin-based platinum(IV) complexes. Both the synthesized PARPi ligands and PARPi-Pt conjugates [PARPi-Pt(IV)] show inhibitory effects against PARP-1's catalytic activity. The PARPi-Pt(IV) conjugates are cytotoxic in a panel of human cancer cell lines, and the leading ones display the ability to overcome cisplatin resistance. A mechanistic investigation reveals that the representative PARPi-Pt(IV) conjugates efficiently enter cells, bind to genomic DNA, disturb cell cycle distribution, and induce apoptotic cell death in both cisplatin-sensitive and-resistant cells. Our study provides a strategy to improve the cytotoxicity of platinum(IV)-based anticancer complexes and overcome cisplatin resistance by using a small-molecule anticancer complex that simultaneously damages DNA and inhibits PARP.

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