184102-76-9 Usage
Explanation
Different sources of media describe the Explanation of 184102-76-9 differently. You can refer to the following data:
1. The compound consists of 11 carbon atoms, 9 hydrogen atoms, 1 chlorine atom, and 1 oxygen atom.
2. This name highlights the presence of a methyl group attached at the third carbon position in the 1H-indene-2-carbonyl chloride structure.
3. The compound is derived from 1H-indene-2-carbonyl chloride by introducing a chlorine atom.
4. The methyl group is attached to the third carbon in the compound's structure.
5. The compound is used as a reactive intermediate for the preparation of various other compounds.
6. 1H-Indene-2-carbonylchloride,3-methyl-(9CI) may be used as a building block for the synthesis of potential drug candidates or pesticides in these industries.
7. The exact properties and uses of the compound may vary depending on the specific application and the synthesis route employed.
Chlorinated derivative
1H-indene-2-carbonyl chloride
Methyl group position
3rd carbon
Application
Organic synthesis
Industries
Pharmaceutical and agrochemical
Property variation
Synthesis route and application
Check Digit Verification of cas no
The CAS Registry Mumber 184102-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,1,0 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 184102-76:
(8*1)+(7*8)+(6*4)+(5*1)+(4*0)+(3*2)+(2*7)+(1*6)=119
119 % 10 = 9
So 184102-76-9 is a valid CAS Registry Number.
184102-76-9Relevant articles and documents
Modular Cyclopentenone Synthesis through the Catalytic Molecular Shuffling of Unsaturated Acid Chlorides and Alkynes
Lee, Yong Ho,Denton, Elliott H.,Morandi, Bill
supporting information, p. 20948 - 20955 (2020/12/21)
We describe a general strategy for the intermolecular synthesis of polysubstituted cyclopentenones using palladium catalysis. Overall, this reaction is achieved via a molecular shuffling process involving an alkyne, an α,β-unsaturated acid chloride, which serves as both the alkene and carbon monoxide source, and a hydrosilane to create three new C-C bonds. This new carbon monoxide-free pathway delivers the products with excellent yields. Furthermore, the regioselectivity is complementary to conventional methods for cyclopentenone synthesis. In addition, a set of regio- and chemodivergent reactions are presented to emphasize the synthetic potential of this novel strategy.
Antiarrythmic and cardioprotective substituted indenoylguanidines
-
, (2008/06/13)
Indenoylguanidines of formula I and formula II, the process for their preparation, their use as medicaments, medicaments containing them, their use as diagnostic agents and medicaments containing them are described. Compounds I are useful for treating cardiac arrhythmias. Further they are useful as cardioprotective agents in mammals, which comprises administering the compound of formula-I or II with the above properties in combination with pharmaceutically accepted carrier to said mammal. STR1
