65399-01-1 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
4-METHYL-2,3-DIHYDRO-ISOINDOL-1-ONE serves as a crucial building block in the synthesis of various pharmaceuticals and agrochemicals. Its chemical structure provides a foundation for the development of new drugs and pesticides, enhancing the range of treatment options and pest control methods available.
Used in Polymer Production:
4-METHYL-2,3-DIHYDRO-ISOINDOL-1-ONE is also utilized in the production of different types of polymers, contributing to the creation of materials with diverse properties and applications in industries such as plastics, textiles, and coatings.
Used in Fragrance Industry:
4-METHYL-2,3-DIHYDRO-ISOINDOL-1-ONE is employed as a fragrance ingredient in the formulation of perfumes and personal care products. Its aromatic properties allow it to contribute to the scent profiles of these products, enhancing their appeal to consumers.
Used in Research and Development:
4-METHYL-2,3-DIHYDRO-ISOINDOL-1-ONE has been studied for its potential pharmacological properties, such as its ability to act as a selective serotonin reuptake inhibitor. This research avenue explores its possible therapeutic applications in treating conditions related to serotonin levels, such as depression and anxiety disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 65399-01-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,9 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65399-01:
(7*6)+(6*5)+(5*3)+(4*9)+(3*9)+(2*0)+(1*1)=151
151 % 10 = 1
So 65399-01-1 is a valid CAS Registry Number.
65399-01-1Relevant academic research and scientific papers
Palladium-Catalyzed Direct C-H Carbonylation of Free Primary Benzylamines: A Synthesis of Benzolactams
Zhang, Chunhui,Ding, Yongzheng,Gao, Yuzhen,Li, Shangda,Li, Gang
supporting information, p. 2595 - 2598 (2018/05/22)
A protocol for palladium-catalyzed C-H carbonylation of readily available free primary benzylamines using NH2 as the chelating group under an atmospheric pressure of CO has been achieved, providing a general, atom- and step-economic approach to
Traceless Directing Group Assisted Cobalt-Catalyzed C?H Carbonylation of Benzylamines
Ling, Fei,Ai, Chongren,Lv, Yaping,Zhong, Weihui
supporting information, p. 3707 - 3712 (2017/10/07)
The first example of cobalt-catalyzed C(sp2)?H carbonylation of benzylamines using a traceless directing group is reported, which was successfully applied to the synthesis of N?unprotected iso-indolinones through direct C?H/N?H bonds activation. This protocol tolerates a variety of functional groups and provides a facile and efficient method for the formal synthesis of (+)-garenoxacin. (Figure presented.).
