60132-21-0 Usage
Uses
Used in Chemical Industry:
(6R,17S,2E,4Z,8Z,10E,14E,18E,20E)-20-(Carboxymethyl)-6-methoxy-2,5,17-trimethyl-2,4,8,10,14,18,20-docosaheptenedioic acid is used as a building block for the synthesis of more complex molecules and materials, due to its versatile structure and functional groups.
Used in Biochemical Research:
In biochemistry, (6R,17S,2E,4Z,8Z,10E,14E,18E,20E)-20-(Carboxymethyl)-6-methoxy-2,5,17-trimethyl-2,4,8,10,14,18,20-docosaheptenedioic acid can be utilized as a probe or a component in the study of various biological processes, potentially interacting with proteins or other biomolecules due to its functional groups.
Used in Pharmaceutical Development:
The unique structure and functional groups of (6R,17S,2E,4Z,8Z,10E,14E,18E,20E)-20-(Carboxymethyl)-6-methoxy-2,5,17-trimethyl-2,4,8,10,14,18,20-docosaheptenedioic acid make it a candidate for drug development, where it could be modified or used as a precursor for the creation of new pharmaceutical agents.
Used in Drug Delivery Systems:
Similar to gallotannin, (6R,17S,2E,4Z,8Z,10E,14E,18E,20E)-20-(Carboxymethyl)-6-methoxy-2,5,17-trimethyl-2,4,8,10,14,18,20-docosaheptenedioic acid could be employed in the development of drug delivery systems, where its functional groups and long carbon chain might enhance the delivery, bioavailability, and therapeutic outcomes of various drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 60132-21-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,3 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 60132-21:
(7*6)+(6*0)+(5*1)+(4*3)+(3*2)+(2*2)+(1*1)=70
70 % 10 = 0
So 60132-21-0 is a valid CAS Registry Number.
InChI:InChI=1/C28H38O7/c1-21(15-18-24(19-26(29)30)20-27(31)32)13-11-9-7-5-6-8-10-12-14-25(35-4)22(2)16-17-23(3)28(33)34/h6,8-12,15-19,21,25H,5,7,13-14,20H2,1-4H3,(H,29,30)(H,31,32)(H,33,34)/b8-6+,11-9+,12-10-,18-15+,22-16-,23-17+,24-19+
60132-21-0Relevant articles and documents
Total synthesis of iso- and bongkrekic acids: Natural antibiotics displaying potent antiapoptotic properties
Francais, Antoine,Leyva-Perez, Antonio,Etxebarria-Jardi, Gorka,Pena, Javier,Ley, Steven V.
experimental part, p. 329 - 343 (2011/03/21)
For over five decades, owing to their antiapoptotic activities, bongkrekic and isobongkrekic acids have generated interest from the scientific community. Here, we disclose full details of our investigation into the synthesis of isobongkrekic acid, which culminated in its first preparation and features various palladium-catalysed cross-couplings and Takai olefination reactions. Access to bongkrekic acid is also reported by this route. These syntheses involve the preparation and use of new general building blocks which could find wider applications. Iso-bong: A versatile first synthesis of isobongkrekic acid (IBA) has been developed. Key steps include three different palladium cross-couplings and an asymmetric homopropargylation. In-depth synthetic studies reveal the challenges faced in generating the right geometry of each diene.
Total synthesis of the anti-apoptotic agents Iso- And bongkrekic acids
Francais, Antoine,Leyva, Antonio,Etxebarria-Jardi, Gorka,Ley, Steven V.
supporting information; experimental part, p. 340 - 343 (2010/03/25)
(Figure presented) The first convergent total synthesis of isobongkrekic acid is reported involving three different stereospecific palladium cross-couplings for the formation of the diene units. Access to bongkrekic acid by this route is also demonstrated. These syntheses involve the formation of several potentially general building blocks.
