878778-84-8 Usage
Uses
Used in Pharmaceutical Industry:
4-AMINOMETHYL QUINOLINE HYDROCHLORIDE is used as a key intermediate in the synthesis of various drugs for its antimalarial and antitumor properties, contributing to the development of new medications that target these conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 4-AMINOMETHYL QUINOLINE HYDROCHLORIDE is utilized as a component in the production of agrochemicals, leveraging its chemical structure to create compounds that can address agricultural challenges.
Used in Neurodegenerative Disease Research:
4-AMINOMETHYL QUINOLINE HYDROCHLORIDE is used as a potential therapeutic agent in the research and treatment of neurodegenerative diseases such as Alzheimer's and Parkinson's, due to its studied effects that may help in managing these conditions.
Used in Drug Development:
As a compound with demonstrated biological activity, 4-AMINOMETHYL QUINOLINE HYDROCHLORIDE is used in drug development for its potential to be incorporated into new pharmaceutical formulations that can treat a range of diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 878778-84-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,8,7,7 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 878778-84:
(8*8)+(7*7)+(6*8)+(5*7)+(4*7)+(3*8)+(2*8)+(1*4)=268
268 % 10 = 8
So 878778-84-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2.ClH/c11-7-8-5-6-12-10-4-2-1-3-9(8)10;/h1-6H,7,11H2;1H
878778-84-8Relevant articles and documents
Fabrication of ω-Transaminase@Metal-Organic Framework Biocomposites for Efficiently Synthesizing Benzylamines and Pyridylmethylamines
Yu, Jinhai,Zong, Weilu,Ding, Yingying,Liu, Junzhong,Chen, Lina,Zhang, Hongjuan,Jiao, Qingcai
, p. 380 - 390 (2021/11/05)
In this study, ten ω-transaminases (ω-TAs) have been investigated to efficiently catalyze the synthesis of twenty-four functionalized benzylamines and pyridylmethylamines. We optimized the reactions, screened suitable amino donors and compared ω-transaminases activities for all aromatic aldehyde substrates. Under the optimized conditions, eighteen aromatic amines have been obtained with 60.4%–96.6% conversions and isolated only via simple extraction and recrystallization with 18.5%–81% yields on a preparative scale. Furthermore, we first immobilized the Bm-STA onto the MOFs via the physical adsorption to overcome the limitation of free enzyme and improve their industrial applications. The obtained Bm-STA/UiO-66-NH2 composites exhibited not only high enzymes loading (80.4 mg g?1) and enzyme activity recovery (95.8%), but also the better reusability, storage stability, pH stability and the tolerance to acetone and DMF.
