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1198299-72-7

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1198299-72-7 Usage

Description

Lenalidomide Impurity 14, also known as 5-Amino-4-(4-nitro-1-oxoisoindolin-2-yl)-5-oxopentanoic Acid, is an impurity found in Lenalidomide (L328000), an immunomodulatory drug that is an analog of Thalidomide. It is a chemical compound that may be present during the manufacturing process of Lenalidomide and is important to monitor and control for quality assurance and patient safety.

Uses

Used in Pharmaceutical Industry:
Lenalidomide Impurity 14 is used as a reference material for the development and validation of analytical methods in the pharmaceutical industry. It helps in the identification, quantification, and control of impurities in Lenalidomide, ensuring the quality and safety of the final drug product.
Used in Quality Control:
Lenalidomide Impurity 14 is used as a quality control standard to assess the performance of analytical methods and to ensure the accuracy and reliability of test results. It is essential for maintaining the quality of Lenalidomide and other related drug products.
Used in Research and Development:
Lenalidomide Impurity 14 is used as a research tool in the development of new drugs and therapies related to Lenalidomide. It can be used to study the chemical and biological properties of the impurity, as well as its potential effects on the efficacy and safety of Lenalidomide.
Used in Regulatory Compliance:
Lenalidomide Impurity 14 is used to meet regulatory requirements for the characterization and control of impurities in drug products. It is essential for pharmaceutical companies to demonstrate compliance with guidelines and regulations related to drug quality and safety.
Used in Drug Safety Assessment:
Lenalidomide Impurity 14 is used in the assessment of potential risks associated with the presence of impurities in Lenalidomide. It helps in understanding the potential impact of the impurity on the safety and efficacy of the drug, allowing for appropriate risk management strategies to be developed and implemented.

Check Digit Verification of cas no

The CAS Registry Mumber 1198299-72-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,2,9 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1198299-72:
(9*1)+(8*1)+(7*9)+(6*8)+(5*2)+(4*9)+(3*9)+(2*7)+(1*2)=217
217 % 10 = 7
So 1198299-72-7 is a valid CAS Registry Number.

1198299-72-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-carbamoyl-4-(4-nitro-1-oxo-1,3-dihydroisoindol-2-yl)butyric acid

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:1198299-72-7 SDS

1198299-72-7Upstream product

1198299-72-7Relevant articles and documents

METHODS FOR SYNTHESIZING 3-(SUBSTITUTED DIHYDROISOINDOLINONE-2-YL)-2,6-DIOXOPIPERIDINE, AND INTERMEDIATES THEREOF

-

Page/Page column 53, (2010/12/29)

The present invention discloses methods for synthesizing 3-(substituted dihydroisoindolinone-2-yl)-2,6-dioxopiperidine and intermediates thereof, namely, the synthesis of compounds of the Formula (I), with each substitutional group defined in the patent specification. Owing to the advantages of high productivity, little influence to the environment and material accessibility, the methods of the present invention is suitable for industrial production.

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