74572-30-8 Usage
Uses
Used in Pharmaceutical Applications:
4,6-dichloroisoindolin-1-one is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and chemical properties contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Applications:
In the agrochemical industry, 4,6-dichloroisoindolin-1-one serves as an important intermediate for the synthesis of various agrochemicals, such as pesticides and herbicides. Its chemical properties enable the creation of effective and targeted agrochemicals for crop protection and management.
Used in Organic Synthesis:
4,6-dichloroisoindolin-1-one is utilized as a building block in the synthesis of a wide range of organic compounds. Its interesting physical and chemical characteristics make it a valuable component in the development of new materials and compounds in organic chemistry.
Used in Material Development:
Due to its unique structural and chemical properties, 4,6-dichloroisoindolin-1-one plays a significant role in the development of new materials and compounds. It serves as a crucial component in the creation of innovative materials with potential applications in various industries, such as electronics, plastics, and coatings.
Check Digit Verification of cas no
The CAS Registry Mumber 74572-30-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,5,7 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 74572-30:
(7*7)+(6*4)+(5*5)+(4*7)+(3*2)+(2*3)+(1*0)=138
138 % 10 = 8
So 74572-30-8 is a valid CAS Registry Number.
74572-30-8Relevant academic research and scientific papers
Ling, Fei,Ai, Chongren,Lv, Yaping,Zhong, Weihui
, p. 3707 - 3712 (2017)
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.).
