1956382-58-3 Usage
Uses
Used in Pharmaceutical Research and Development:
Methyl 3-aminoquinoline-5-carboxylate is utilized as a key building block in the synthesis of pharmaceutical compounds. Its unique structure and reactivity allow for the creation of new drug candidates with potential therapeutic applications.
Used in Agrochemical Development:
In the agrochemical industry, methyl 3-aminoquinoline-5-carboxylate serves as a crucial intermediate for the development of new agrochemicals. Its properties make it suitable for the synthesis of molecules with pesticidal or herbicidal activities, contributing to more effective crop protection strategies.
Used in Organic Synthesis:
Methyl 3-aminoquinoline-5-carboxylate is employed as a versatile intermediate in organic synthesis. Its ability to participate in various chemical reactions makes it a valuable component in the preparation of a wide range of organic compounds with diverse applications.
Used in Medicinal Chemistry:
As a significant compound in medicinal chemistry, methyl 3-aminoquinoline-5-carboxylate is used for the synthesis of biologically active molecules. Its potential to contribute to the development of new medicines makes it an essential tool in the advancement of medical treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 1956382-58-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,9,5,6,3,8 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1956382-58:
(9*1)+(8*9)+(7*5)+(6*6)+(5*3)+(4*8)+(3*2)+(2*5)+(1*8)=223
223 % 10 = 3
So 1956382-58-3 is a valid CAS Registry Number.
1956382-58-3Relevant academic research and scientific papers
Synthesis method of 3-aminoquinoline-5-carboxylic acid methyl ester
-
Paragraph 0012; 0014-0015, (2021/01/15)
The invention discloses a synthesis method of 3-aminoquinoline-5-carboxylic acid methyl ester. The method comprises the following steps: carrying out a bromination reaction on 3-aminoquinoline servingas a raw material and bromine to obtain 3-amino-5-bromoquinoline, and carrying out a carbonyl insertion reaction to obtain the 3-aminoquinoline-5-carboxylic acid methyl ester. The method is simple insynthetic route, reasonable in process selection, simple and easily available in raw materials, convenient to operate and post-treat, relatively high in total yield and easy to amplify, and can be used for large-scale production.
QUINOLINE DERIVATIVES AS ALPHA4BETA7 INTEGRIN INHIBITORS
-
, (2020/05/28)
The present disclosure provides a compound of Formula (I) or a pharmaceutically acceptable salt thereof as described herein. The present disclosure also provides pharmaceutical compositions comprising a compound of Formula (I), processes for preparing compounds of Formula (I), and therapeutic methods for treating inflammatory disease.
