19123-67-2 Usage
Uses
Used in Plant Growth Regulation:
Isogibberellic Acid is used as a plant growth regulator for promoting growth and development in various plant species. Its application reason is based on its structural similarity to Gibberellic Acid, which is a naturally occurring plant hormone that plays a crucial role in regulating plant growth and development. By mimicking the action of Gibberellic Acid, Isogibberellic Acid can enhance plant growth, increase yield, and improve overall plant health.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, Isogibberellic Acid is used as a precursor for the synthesis of various drugs and pharmaceutical compounds. Its unique molecular structure and functional groups make it a versatile building block for the development of new drugs with potential therapeutic applications.
Used in Agricultural Industry:
Isogibberellic Acid is used as a growth-promoting agent in the agricultural industry for improving crop yield and quality. Its application reason is due to its ability to stimulate plant growth, enhance nutrient uptake, and increase resistance to various stress factors, such as drought, salinity, and disease. By incorporating Isogibberellic Acid into fertilizers or plant growth formulations, farmers can achieve better crop performance and higher productivity.
Check Digit Verification of cas no
The CAS Registry Mumber 19123-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,2 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 19123-67:
(7*1)+(6*9)+(5*1)+(4*2)+(3*3)+(2*6)+(1*7)=102
102 % 10 = 2
So 19123-67-2 is a valid CAS Registry Number.
19123-67-2Relevant academic research and scientific papers
1β-Hydroxygibberellin A5. Preparation and Comparison with Gibberellin A3
Kirkwood, Paul S.,MacMillan, Jake,Hutchison, Michael
, p. 707 - 712 (2007/10/02)
The preparation of 1β-hydroxygibberellin A5 from gibberellin A3 is described.Unlike its naturally occurring allylic isomer gibberellin A3, 1β-hydroxygibberellin A5 is stable to aqueous alkali and acid-catalysed aromatisation of ring A does not occur.Reasons for these differences, and for the hitherto unreported 3-epimerisation of gibberellin A3 by base, are discussed in terms of O-alkyl fission of the lactone bridge.
