10500-64-8 Usage
Description
4-[(7-Chloro-4-quinolinyl)amino]-1-pentanol is an organic compound with a chemical structure that features a pentanol backbone and a 7-chloro-4-quinolinyl amino group. It is a yellow solid, which indicates its stability and potential for use in various applications.
Uses
Used in Pharmaceutical Industry:
4-[(7-Chloro-4-quinolinyl)amino]-1-pentanol is used as an intermediate in the preparation of Cletoquine Oxalate and Chloroquinolin. These compounds are known for their antimalarial properties and are used to treat and prevent malaria infections. The intermediate plays a crucial role in the synthesis of these drugs, contributing to their development and production.
Used in Chemical Synthesis:
As a chemical intermediate, 4-[(7-Chloro-4-quinolinyl)amino]-1-pentanol can be utilized in the synthesis of various other compounds with potential applications in different industries. Its unique structure allows for further chemical reactions and modifications, making it a versatile building block for the creation of new molecules with specific properties and uses.
Check Digit Verification of cas no
The CAS Registry Mumber 10500-64-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,0 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10500-64:
(7*1)+(6*0)+(5*5)+(4*0)+(3*0)+(2*6)+(1*4)=48
48 % 10 = 8
So 10500-64-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H17ClN2O/c1-10(3-2-8-18)17-13-6-7-16-14-9-11(15)4-5-12(13)14/h4-7,9-10,18H,2-3,8H2,1H3,(H,16,17)
10500-64-8Relevant articles and documents
Preparation method of hydroxychloroquine impurity
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Paragraph 0056-0059; 0068-0071; 0080-0083; 0092-0095, (2020/08/22)
The invention discloses a preparation method of a hydroxychloroquine impurity. 4-amino-1-pentanol taken as a raw material undergoes a five-step reaction to realize synthesis of a hydroxychloroquine impurity VIII. The preparation method is reasonable in process design and high in operability, and industrial production can be realized; reagents used in the synthesis method are simple and easy to obtain; the purity of the hydroxychloroquine impurity obtained through the reaction can reach 98% or above, and the total yield can reach 20% or above. The hydroxychloroquine impurity prepared by the invention provides an important basis for scientific evaluation of quality, safety and efficiency of hydroxychloroquine.