5632-16-6 Usage
Uses
Used in Pharmaceutical Industry:
4-Bromomethylquinoline is used as a key building block for the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique structure allows for the creation of diverse chemical entities with potential medicinal properties.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Bromomethylquinoline serves as an intermediate in the synthesis of various agrochemicals, including pesticides and herbicides. Its incorporation into these compounds can enhance their effectiveness in controlling pests and weeds, thereby supporting agricultural productivity.
Used in Dye and Pigment Production:
4-Bromomethylquinoline is utilized as an intermediate in the production of dyes and pigments, particularly those requiring specific color characteristics and stability. Its presence in these compounds can improve their performance in various applications, such as textiles, plastics, and printing inks.
Used in Specialty Chemicals:
4-Bromomethylquinoline also finds application in the synthesis of specialty chemicals, where its unique properties can be harnessed to create compounds with specific functions or improved performance in various industrial processes.
Safety Precautions:
Given its classification as a hazardous substance, 4-Bromomethylquinoline requires careful handling and storage to ensure safety. Proper safety measures should be implemented to minimize risks associated with its use, including the adoption of appropriate personal protective equipment and adherence to established safety protocols.
Check Digit Verification of cas no
The CAS Registry Mumber 5632-16-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,3 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5632-16:
(6*5)+(5*6)+(4*3)+(3*2)+(2*1)+(1*6)=86
86 % 10 = 6
So 5632-16-6 is a valid CAS Registry Number.
5632-16-6Relevant academic research and scientific papers
Synthesis and biological activity of new 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase inhibitors: 2-oxetanones with a side chain mimicking the folded structure of 1233A.
Hashizume,Ito,Yamada,Nagashima,Kanao,Tomoda,Sunazuka,Kumagai,Omura
, p. 512 - 520 (2007/10/02)
To mimic the folded side chain conformation of 1233A (1), which is a 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase inhibitor, 1233A analogs with aromatic rings in the side chain were synthesized. The 2-oxetanone moiety was kept intact. Among 1233A and its synthetic analogs, trans-3-hydroxymethyl-4-[2-(7-methoxycarbonyl-1-naphthyl)ethyl]-2-oxe tanone (23) showed the highest HMG-CoA synthase inhibitory activity in vitro. The structure-activity relationship at the side chain is discussed.
