1025424-03-6 Usage
Uses
Used in Pharmaceutical Industry:
1H-Isoindole, 2,3-dihydro-4-methoxy-2-[(4-methylphenyl)sulfonyl]is used as a potential pharmaceutical candidate for the development of new drugs. Its unique structure and reactivity may allow for the design of novel therapeutic agents with specific target interactions, potentially leading to the treatment of various diseases and conditions.
Used in Agrochemical Industry:
1H-Isoindole, 2,3-dihydro-4-methoxy-2-[(4-methylphenyl)sulfonyl]is used as a potential component in the development of agrochemicals, such as pesticides or herbicides. Its structural properties and reactivity may contribute to the creation of effective and targeted agrochemicals, enhancing crop protection and yield.
Further research and evaluation of 1H-Isoindole, 2,3-dihydro-4-methoxy-2-[(4-methylphenyl)sulfonyl]are necessary to explore its full potential and optimize its applications in various industries. This includes understanding its chemical properties, reactivity, and interactions with biological systems, as well as assessing its safety and efficacy in practical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1025424-03-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,5,4,2 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1025424-03:
(9*1)+(8*0)+(7*2)+(6*5)+(5*4)+(4*2)+(3*4)+(2*0)+(1*3)=96
96 % 10 = 6
So 1025424-03-6 is a valid CAS Registry Number.
1025424-03-6Relevant articles and documents
SAR studies of capsazepinoid bronchodilators. Part 1: The importance of the catechol moiety and aspects of the B-ring structure
Dalence-Guzman, Maria F.,Berglund, Magnus,Skogvall, Staffan,Sterner, Olov
, p. 2499 - 2512 (2008/09/21)
Capsazepine as well as its derivatives and analogues are general inhibitors of constriction of human small airways. From a systematic variation of the capsazepine structure, divided into four regions, SARs were established. This part concerns the catechol moiety of the A-ring as well as the 2,3,4,5-tetrahydro-1H-2-azepine moiety (the B-ring) of capsazepine. It is revealed that a conformational constrain (as a fused ring) is important and that compounds with a six-membered B-ring (as a 1,2,3,4-tetrahydroisoquinoline) in general are more potent than the corresponding isoindoline, 2,3,4,5-tetrahydro-1H-2-benzazepine and 2,3,4,5-tetrahydro-1H-3-benzazepine derivatives.
