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22S,23S-Epicastasterone is a naturally occurring brassinosteroid, which is a group of plant hormones that play a crucial role in regulating plant growth and development. It possesses a unique chemical structure that allows it to interact with specific receptors in plants, modulating their growth and development processes.

72050-69-2

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72050-69-2 Usage

Uses

Used in Plant Growth Regulation:
22S,23S-Epicastasterone is used as a reactant/reagent for the preparation of indolylacetoxy brassinosteroids, which are known for their plant growth-regulating activity. These compounds can enhance various aspects of plant growth, such as cell elongation, division, and differentiation, leading to improved crop yields and quality.
Used in Agricultural Industry:
In the agricultural industry, 22S,23S-Epicastasterone is used as a growth regulator to promote healthy plant growth and development. Its application can lead to increased resistance against environmental stresses, such as drought, salinity, and temperature fluctuations, ultimately resulting in better crop productivity and resilience.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, 22S,23S-Epicastasterone, due to its hormonal properties, may also have potential applications in the pharmaceutical industry. It could be used as a starting material for the synthesis of other bioactive compounds or as a research tool to study the effects of brassinosteroids on human health and disease.

Check Digit Verification of cas no

The CAS Registry Mumber 72050-69-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,0,5 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 72050-69:
(7*7)+(6*2)+(5*0)+(4*5)+(3*0)+(2*6)+(1*9)=102
102 % 10 = 2
So 72050-69-2 is a valid CAS Registry Number.

72050-69-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 22(S),23(S),24-epicastasterone

1.2 Other means of identification

Product number -
Other names 24-epicastasterone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:72050-69-2 SDS

72050-69-2Relevant academic research and scientific papers

Synthesis and biological activity of brassinolide and its 22 beta, 23 beta-isomer: novel plant growth-promoting steroids.

Thompson,Mandava,Meudt,Lusby,Spaulding

, p. 567 - 580 (2007/10/02)

Brassinolide (2 alpha, 3 alpha, 22 alpha, 23 alpha-tetrahydroxy-24 alpha-methyl -B-homo-7-oxa-5 alpha-cholestan-6-one), a novel plant growth-promoting steroid isolated from rape pollen, and its hitherto unknown 22 beta, 23 beta-isomer were synthesized from a C-24 epimeric 60:40 mixture of 22-dehydroxampesterol (24 alpha-methyl) and brassicasterol (24 beta-methyl) from oysters. The method of synthesis favored the formation of the 22 beta, 23 beta-isomer by better than 4:1. Comparative plant growth-promoting capabilities of brassinolide, both natural and synthetic, and its three side chain cis-glycolic isomers in the bean second internode bioassay showed that the natural and synthetic brassinolides were equally active and caused splitting of the internode at the 0.1 microgram level. The least active was the 22 beta, 23 beta-isomer of brassinolide. The isomers with the 22 alpha, 23 alpha and 24 alpha, and the 22 beta, 23 beta and 24 beta configurations were highly active and were required at about 10 times the concentration of brassinolide to cause the same physiological response. In the bean first internode bioassay, an auxin-induced growth test system which employs isolated bean plant segments, the isomer with 22 beta, 23 beta and 24 beta configuration caused a greater response than brassinolide. Two of the four tetrahydroxy ketones obtained in the synthesis of the isomers were also active in both assays.

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