916756-04-2 Usage
Main properties
1. Chemical name: 5H-Indeno[1,2-b]quinoline-9,11-dione, 6,7,8,10-tetrahydro-7,7-dimethyl-5-phenyl-10-(phenylmethyl)-
2. Fused ring structure: Contains a quinoline backbone with a dione functional group and a pentacyclic ring system
3. Functional groups: Two methyl groups, two phenyl groups, and a phenylmethyl group attached to the ring structure
4. Potential applications: May have biological and pharmaceutical applications due to its unique structure and functional groups
5. Risks: May pose risks to human health and the environment, should be handled and used with caution
Specific content
1. Chemical name: 5H-Indeno[1,2-b]quinoline-9,11-dione, 6,7,8,10-tetrahydro-7,7-dimethyl-5-phenyl-10-(phenylmethyl)-
2. Fused ring structure: Quinoline backbone with dione functional group and pentacyclic ring system
3. Functional groups: Two methyl groups, two phenyl groups, and a phenylmethyl group attached
4. Applications: Potential biological and pharmaceutical applications
5. Risks: Potential risks to human health and environment, handle with caution
Check Digit Verification of cas no
The CAS Registry Mumber 916756-04-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,7,5 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 916756-04:
(8*9)+(7*1)+(6*6)+(5*7)+(4*5)+(3*6)+(2*0)+(1*4)=192
192 % 10 = 2
So 916756-04-2 is a valid CAS Registry Number.
916756-04-2Relevant academic research and scientific papers
Efficient and direct synthesis of poly-substituted indeno1[1,2-b]quinolines assisted by p-toluene sulfonic acid using high-temperature water and microwave heating via one-pot, three-component reaction
Tu, Shu-Jiang,Jiang, Bo,Zhang, Jun-Yong,Jia, Run-Hong,Zhang, Yan,Yao, Chang-Sheng
, p. 3980 - 3985 (2008/09/18)
Reactions of aldehydes, 1,3-indanedione and enaminones were successfully carried out using p-toluene sulfonic acid (p-TsOH) as a catalyst and high-temperature water as a solvent under microwave irradiation. This method provided several advantages such as
