100322-43-8 Usage
Description
3-isobutyl-9,10-dimethoxy-3,4,6,7-tetrahydro-2H-benzo[a]quinolizine-2-one is a complex organic compound with a unique molecular structure. It is characterized by its isobutyl group at the 3-position, two methoxy groups at the 9 and 10 positions, and a tetrahydro-2H-benzo[a]quinolizine-2-one core. 3-isobutyl-9,10-dimethoxy-3,4,6,7-tetrahydro-2H-benzo[a]quinolizine-2-one has potential applications in various fields due to its specific chemical properties and structural features.
Uses
Used in Pharmaceutical Industry:
3-isobutyl-9,10-dimethoxy-3,4,6,7-tetrahydro-2H-benzo[a]quinolizine-2-one is used as a pharmaceutical compound for its potential therapeutic effects. The compound's unique structure may allow it to interact with specific biological targets, making it a candidate for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, 3-isobutyl-9,10-dimethoxy-3,4,6,7-tetrahydro-2H-benzo[a]quinolizine-2-one can be used as a starting material or intermediate for the synthesis of other complex organic molecules. Its unique structural features may enable the development of novel chemical entities with various applications.
Used in Material Science:
The compound may also find applications in material science, where its specific properties could be utilized in the development of new materials with tailored characteristics. For example, its structural features might contribute to the creation of materials with specific optical, electronic, or mechanical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 100322-43-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,3,2 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 100322-43:
(8*1)+(7*0)+(6*0)+(5*3)+(4*2)+(3*2)+(2*4)+(1*3)=48
48 % 10 = 8
So 100322-43-8 is a valid CAS Registry Number.
100322-43-8Relevant articles and documents
Structural requirement of C11b chirality of tetrabenazine analogs as VMAT2 imaging ligands: synthesis and in vivo evaluation
Xue, Danlu,Liu, Chunyi,Li, Xiaomin,Tang, Jie,Cao, Lihua,Liu, Yi,Chen, Zhengping
, p. 419 - 428 (2017)
We studied on the structural requirement of C11b chirality of tetrabenazine (TBZ) analogs as vesicular monoamine transporter 2 (VMAT2) ligands. TBZ analogs (2, 6a, 6b) and 18F-radiolabeled [18F]6a and [18F]6b with eliminat
A novel reaction of cyanogen iodide with cyclic tertiary amines
Lee, Byung H.,Clothier, Michael F.,Pickering, Dacia A.
, p. 6119 - 6122 (1997)
It has been shown that cyanogen iodide reacts with the tertiary amine ring of marcfortine A (1) to give cyano (4) and iodocyano (3) substituted products. We have now extended this reaction to various cyclic tertiary amines.
