4955-22-0 Usage
Uses
Used in Plant Growth Regulation:
2β-Hydroxy-1β,4aα-dimethyl-8-methylenegibbane-1α,10β-dicarboxylic acid is used as a regulatory molecule in the agricultural industry for its role in plant growth and development. As a derivative of gibberellins, it is involved in cell growth and elongation, and it can potentially influence gene transcription levels, making it a valuable tool for enhancing crop yields and improving plant resistance to various stress factors.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2β-Hydroxy-1β,4aα-dimethyl-8-methylenegibbane-1α,10β-dicarboxylic acid may be used as a starting material for the synthesis of novel compounds with potential therapeutic applications. Its unique structure and functional groups could be exploited to develop new drugs targeting specific diseases or conditions.
Used in Chemical Synthesis:
2β-Hydroxy-1β,4aα-dimethyl-8-methylenegibbane-1α,10β-dicarboxylic acid can be utilized as an intermediate in the synthesis of various chemical products, such as specialty chemicals, fragrances, or additives. Its versatile structure and functional groups make it a promising candidate for the development of new materials with specific properties.
Used in Analytical Chemistry:
2β-Hydroxy-1β,4aα-dimethyl-8-methylenegibbane-1α,10β-dicarboxylic acid may also find applications in analytical chemistry as a reference material or standard for the development and validation of analytical methods. Its unique structure and properties could be useful for testing the performance of chromatographic, spectroscopic, or other analytical techniques.
Check Digit Verification of cas no
The CAS Registry Mumber 4955-22-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,5 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4955-22:
(6*4)+(5*9)+(4*5)+(3*5)+(2*2)+(1*2)=110
110 % 10 = 0
So 4955-22-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H28O5/c1-10-8-20-9-11(10)4-5-12(20)18(2)7-6-13(21)19(3,17(24)25)15(18)14(20)16(22)23/h11-15,21H,1,4-9H2,2-3H3,(H,22,23)(H,24,25)/t11-,12+,13+,14-,15+,18+,19-,20+/m1/s1
4955-22-0Relevant academic research and scientific papers
Preparation of ent-Gibberellane and 16-epi-ent-Gibberellane
Gaskin, Paul,MacMillan, Jake,Makinson, Ian K.,Willis, Christine L.
, p. 1359 - 1364 (2007/10/02)
A mixture of ent-gibberellane 1 and 16-epi-ent-gibberellane 2, the parent hydrocarbons of the gibberellin plant hormones, has been prepared from gibberellin A14 dimethyl ester 5 by deoxygenation sequentially at carbons 3, 7 and 19 and then hydrogenation.The most direct route proceeded by dehydration of the 3-ol in 5 to the 2-ene 27, hydride reduction to the 7,19-diol 28, hydride reduction of the corresponding 7,19-dimethanesulfonate 29 to the 19-monomethanesulfonate 30, and then hydrolysis to the 19-ol 31 which was converted into the phenyl selenide 38.Hydrogenolysis of the selenide 38, with concomitant hydrogenation of the 2- and 16-double bonds, gave a mixture of ent-gibberellane 1 and 16-epi-ent-gibberellane 2 in the ratio of 73:27.This mixture was separated on the analytical scale by capillary GLC and the two epimers were characterised by GLC-MS to provide reference mass spectra and KRI as fossil markers.The structures 1 and 2 were assigned on the basis that the major component was the endo-16-methyl epimer.
