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618-63-3

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618-63-3 Usage

General Description

3-Chloro-5-nitrophenol is a type of nitrophenol, which are organic compounds that consist of a phenol group and one or more nitro groups. It is a synthetic compound primarily used in the preparation of dyes and pigments, pharmaceuticals, and pesticides. The compound is recognized by its yellow color, and it can form yellow or yellow-orange crystals. Like many chlorinated and nitro aromatic compounds, 3-Chloro-5-nitrophenol is hazardous and poses risks to human health and the environment. It is soluble in water and various organic solvents, and it is stable under normal temperatures and pressures, yet it can react with oxidizing agents.

Check Digit Verification of cas no

The CAS Registry Mumber 618-63-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 618-63:
(5*6)+(4*1)+(3*8)+(2*6)+(1*3)=73
73 % 10 = 3
So 618-63-3 is a valid CAS Registry Number.

618-63-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Chloro-5-nitrophenol

1.2 Other means of identification

Product number -
Other names Phenol, 3-chloro-5-nitro-

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:618-63-3 SDS

618-63-3Relevant articles and documents

COMPOUNDS, COMPOSITIONS AND METHODS OF USE

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Page/Page column 115-116; 141-142; 197; 203, (2020/07/06)

Herein, compounds, compositions and methods for modulating inclusion formation and stress granules in cells related to the onset of neurodegenerative diseases, musculoskeletal diseases, cancer, ophthalmological diseases, and viral infections are described.

Substituted benzodiazepine ring compound and preparation method and application thereof

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Paragraph 0481-0483, (2017/07/22)

The invention discloses a substituted benzodiazepine ring compound and a preparation method and application thereof and further relates to a pharmaceutical composition and application of the compound. According to the substituted benzodiazepine ring compound, the effect of preventing or treating an immune inflammatory disease or tumor is achieved through activation of a selectively antagonistic or collaboratively excited NOD1/2 signal transduction pathway; the substituted benzodiazepine ring compound has a polypeptidase stability and is not degraded by polypeptidase in the organism.

NEW SUBSTITUTED ARYLSULPHONYLGLYCINES, THE PREPARATION THEREOF AND THE USE THEREOF AS PHARMACEUTICAL COMPOSITIONS

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, (2008/12/07)

The present invention relates to substituted arylsulphonylglycines of general formula (I) wherein R, X, Y and Z are defined as in claim 1, the tautomers, enantiomers, diastereomers, mixtures thereof and salts thereof, which have valuable pharmacological properties, particularly the suppression of the interaction of glycogen phosphorylase a with the GL subunit of glycogen-associated protein phosphatase 1 (PP1 ), and their use as pharmaceutical compositions.

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