5508-47-4 Usage
Description
Gibberellin A7 Methyl Ester, a derivative of Gibberellin A7, is a plant hormone that has been isolated from the culture filtrates of the fungus Gibberella fujikuroi. It plays a crucial role in promoting the growth and elongation of plant cells, making it an essential component in various agricultural and horticultural applications.
Uses
Used in Agriculture:
Gibberellin A7 Methyl Ester is used as a growth regulator for promoting cell elongation and growth in plants. It helps in increasing the overall yield and quality of crops by stimulating various physiological processes, such as germination, stem elongation, and fruit development.
Used in Horticulture:
In horticulture, Gibberellin A7 Methyl Ester is used as a growth enhancer to improve the appearance and health of ornamental plants. It can be applied to control plant height, promote flowering, and improve overall plant vigor.
Used in Plant Tissue Culture:
Gibberellin A7 Methyl Ester is also used in plant tissue culture as a growth-promoting agent. It aids in the successful propagation of plants by influencing cell division and elongation, leading to the development of healthy and vigorous plantlets.
Used in Research:
Gibberellin A7 Methyl Ester is utilized in scientific research to study the effects of plant hormones on various aspects of plant growth and development. It helps researchers understand the complex signaling pathways involved in plant growth regulation and can be used to develop new strategies for crop improvement and stress resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 5508-47-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,0 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5508-47:
(6*5)+(5*5)+(4*0)+(3*8)+(2*4)+(1*7)=94
94 % 10 = 4
So 5508-47-4 is a valid CAS Registry Number.
InChI:InChI=1/C23H28ClN3O3/c1-4-21(28)27-15-13-26(14-16-27)19-9-7-18(8-10-19)25-22(29)23(2,3)30-20-11-5-17(24)6-12-20/h5-12H,4,13-16H2,1-3H3,(H,25,29)
5508-47-4Relevant articles and documents
Substitution Reactions of the 3-Epimeric Methanesulphonates of Methyl Gibberellate
Duri, Zvitendo J.,Hanson, James R.
, p. 603 - 607 (2007/10/02)
Whereas displacement of the 3β-(axial)-methylsulphonyloxy group from methyl gibberellate with lithium chloride or buffered aqueous acetone proceeds predominantly with syn rearrangement to afford the 1β-chloro- or 1β-hydroxy-gibberellin, the corresponding 3α-(equatorial) epimer reacts with simple inversion of configuration.This affords on the one hand a facile route to the 1-hydroxygibberellins and, on the other, a means of labelling gibberellins at C-3.
