40163-56-2 Usage
Description
EBURNAMENINE-14-CARBOXYLIC ACID, 14,15-DIHYDRO-14-HYDROXY-, ETHYL ESTER, (3A,14B,16A)is a complex organic compound with a unique molecular structure. It is characterized by its carboxylic acid, dihydro, and hydroxy functional groups, as well as its ester linkage with ethyl. EBURNAMENINE-14-CARBOXYLIC ACID, 14,15-DIHYDRO-14-HYDROXY-, ETHYL ESTER, (3A,14B,16A)-'s stereochemistry is defined by its (3A,14B,16A)configuration, which may influence its properties and potential applications.
Uses
Used in Pharmaceutical Applications:
EBURNAMENINE-14-CARBOXYLIC ACID, 14,15-DIHYDRO-14-HYDROXY-, ETHYL ESTER, (3A,14B,16A)is used as a pharmaceutical compound for its potential therapeutic effects. EBURNAMENINE-14-CARBOXYLIC ACID, 14,15-DIHYDRO-14-HYDROXY-, ETHYL ESTER, (3A,14B,16A)-'s unique structure and functional groups may allow it to interact with biological targets, such as enzymes or receptors, which could be beneficial in the treatment of various diseases or conditions.
Used in Chemical Research:
In the field of chemical research, EBURNAMENINE-14-CARBOXYLIC ACID, 14,15-DIHDRO-14-HYDROXY-, ETHYL ESTER, (3A,14B,16A)can be used as a starting material or intermediate in the synthesis of other complex organic molecules. Its unique structure and functional groups may provide new insights into chemical reactions and mechanisms, contributing to the advancement of chemical science.
Used in Drug Delivery Systems:
Similar to the application of gallotannin in drug delivery systems, EBURNAMENINE-14-CARBOXYLIC ACID, 14,15-DIHYDRO-14-HYDROXY-, ETHYL ESTER, (3A,14B,16A)could potentially be employed in the development of novel drug delivery systems. Its unique structure and functional groups may allow for targeted delivery of therapeutic agents, improving their bioavailability and therapeutic outcomes.
Check Digit Verification of cas no
The CAS Registry Mumber 40163-56-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,1,6 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 40163-56:
(7*4)+(6*0)+(5*1)+(4*6)+(3*3)+(2*5)+(1*6)=82
82 % 10 = 2
So 40163-56-2 is a valid CAS Registry Number.
InChI:InChI=1/C22H28N2O3/c1-3-21-11-7-12-23-13-10-16-15-8-5-6-9-17(15)24(18(16)19(21)23)22(26,14-21)20(25)27-4-2/h5-6,8-9,19,26H,3-4,7,10-14H2,1-2H3/t19-,21+,22+/m1/s1
40163-56-2Relevant articles and documents
A facile one-pot synthesis of vinpocetine
Kuge,Nakazawa,Kometani,Sugaya,Mochida,Tomioka
, p. 759 - 766 (1994)
A one-pot synthesis of vinpocetine from vincamine was established. Lewis acids caused transesterification and/or dehydration of vincamine in EtOH. FeCl3 catalyzed both transesterification and dehydration while Ti(OEt)4 selectively catalyzed transesterification.
Kinetics and mechanisms of vinpocetine degradation in aqueous solutions
Muhammad,Adams,Lee
, p. 126 - 131 (2007/10/02)
Under stressed conditions, vinpocetine (1; ethyl apovincamin-22-oate) equilibrates with vincaminic acid ethyl ester (2) and 14-epivincaminic acid ethyl ester (3), and hydrolyzes to apovincaminic acid (4). Sequentially, 2 is equilibrated with 14-epivincaminic acid ethyl ester (3) and hydrolyzes to vincaminic acid (5), which equilibrates with 4 and 14-epivincaminic acid (6). At acidic pH, the major route of degradation is 1?2→5. However, at neutral pH, the major route of degradation is 1→4?5. The kinetics for the degradation of 1 in the pH 1-3 region is represented by a consecutive reaction with a reversible step (second-order), but the degradation of 1 in the pH 3.5-6.0 region follows pseudo first-order kinetics. Significant buffer catalysis is observed with acetate and phosphate buffers. Reactions are dependent on the ionic strength, pH, and temperature. No oxygen effect on the degradation of vinpocetine is found.
Synthesis of vinca alkaloids and related compounds, VII. Epimerization studies
Kalaus Gy.,Gyulai Zs.,Kajtar-Peredy,et al.
, p. 221 - 230 (2007/10/02)
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