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1H-Isoindole-1,3(2H)-dione, 2-[3-(2-nitrophenoxy)propyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66725-23-3

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66725-23-3 Usage

Appearance

Yellow to brown The compound has a yellow to brown color in its solid form.

Usage

Pharmaceutical intermediate and organic synthesis It is commonly used as an intermediate in the synthesis of pharmaceuticals and other organic compounds.

Functional groups

Nitro group and phenoxy group The presence of these groups makes the compound useful for the production of various drugs and other organic compounds.

Precautions

Harmful if swallowed, inhaled, or in contact with skin The compound should be handled with care to avoid potential health risks.

Storage

Cool, dry, and well-ventilated area away from incompatible substances Proper storage conditions help maintain the stability and safety of the compound.

Check Digit Verification of cas no

The CAS Registry Mumber 66725-23-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,7,2 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 66725-23:
(7*6)+(6*6)+(5*7)+(4*2)+(3*5)+(2*2)+(1*3)=143
143 % 10 = 3
So 66725-23-3 is a valid CAS Registry Number.

66725-23-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[3-(2-nitrophenoxy)propyl]isoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names -

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:66725-23-3 SDS

66725-23-3Upstream product

66725-23-3Relevant academic research and scientific papers

Selective small molecules blocking HIV-1 tat and coactivator PCAF association

Zeng, Lei,Li, Jiaming,Muller, Michaela,Yan, Sherry,Mujtaba, Shiraz,Pan, Chongfeng,Wang, Zhiyong,Zhou, Ming-Ming

, p. 2376 - 2377 (2007/10/03)

Development of drug resistance from mutations in the targeted viral proteins leads to continuation of viral production by chronically infected cells, contributing to HIV-mediated immune dysfunction. Targeting a host cell protein essential for viral reproduction, rather than a viral protein, may minimize the viral drug resistance problem as observed with HIV protease inhibitors. We report here the development of a novel class of N1-aryl-propane-1,3-diamine compounds using a structure-based approach that selectively inhibit the activity of the bromodomain of the human transcriptional co-activator PCAF, of which association with the HIV trans-activator Tat is essential for transcription and replication of the integrated HIV provirus. Copyright

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