20134-29-6 Usage
Uses
Used in Plant Growth Regulation:
4aα-Formyl-2β,7-dihydroxy-1β-methyl-8-methylenegibbane-1α,10β-dicarboxylic acid is used as a plant growth regulator for its ability to modulate the growth and development of plants. As a derivative of Gibberellin, it can influence various plant processes, such as stem elongation, germination, and flowering, making it a valuable tool in agriculture and horticulture.
Used in Pharmaceutical Development:
4aα-Formyl-2β,7-dihydroxy-1β-methyl-8-methylenegibbane-1α,10β-dicarboxylic acid is used as a pharmaceutical candidate due to its complex structure and potential biological activities. The presence of multiple functional groups may allow for interactions with various biological targets, making it a promising compound for the development of new drugs with different therapeutic applications.
Used in Chemical Synthesis:
4aα-Formyl-2β,7-dihydroxy-1β-methyl-8-methylenegibbane-1α,10β-dicarboxylic acid can be used as a starting material or intermediate in the synthesis of other complex organic compounds. Its unique structure and functional groups may enable the development of novel chemical entities with specific properties and applications in various industries, such as materials science, pharmaceuticals, or agrochemicals.
Used in Research and Development:
4aα-Formyl-2β,7-dihydroxy-1β-methyl-8-methylenegibbane-1α,10β-dicarboxylic acid serves as a valuable research tool for studying the structure-activity relationships of Gibberellin derivatives and their potential applications. It can be used to investigate the effects of structural modifications on biological activity, providing insights into the design of more effective and targeted compounds for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 20134-29-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,3 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 20134-29:
(7*2)+(6*0)+(5*1)+(4*3)+(3*4)+(2*2)+(1*9)=56
56 % 10 = 6
So 20134-29-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H26O7/c1-10-7-19-8-20(10,27)6-3-11(19)18(9-21)5-4-12(22)17(2,16(25)26)14(18)13(19)15(23)24/h9,11-14,22,27H,1,3-8H2,2H3,(H,23,24)(H,25,26)/t11-,12-,13+,14+,17+,18+,19-,20-/m0/s1
20134-29-6Relevant academic research and scientific papers
Stokes, Tania S.,Mander, Lewis N.,Croker, Stephen J.,Twitchin, Bruce,Hanke, David E.
, p. 165 - 174 (2003)
Using full scan GC-MS a wide range of gibberellins (GAs) was identified in the young inflorescences of the dioecious species Rumex acetosa L., consistent with the ubiquitous early 13-hydroxylation pathway in both male and female plants. In addition, R. acetosa is the first species in which all three 3β, 13-dihydroxylated C20-GAs - GA18, GA38 and GA23 - have been identified in the same organism, suggesting an early 3β,13-dihydroxylation biosynthesis pathway in this species. Authentic GA18, GA38 and GA23 were synthesized and their effects and that of GA1, a GA common to both pathways, on the time to inflorescence emergence was investigated. GA1 accelerated the emergence of inflorescences in both male and female plants. In addition some evidence for biological activity per se of the C20-GA38 was obtained.
