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105593-21-3

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105593-21-3 Usage

Description

2β,4aα,7,9β-Tetrahydroxy-1-methyl-8-methylenegibbane-1α,10β-dicarboxylic acid 1,4a-lactone is a complex organic compound derived from the gibbane family of diterpenoids. It is characterized by its unique molecular structure with multiple hydroxyl and carboxylic acid functional groups, as well as a methyl group and a methylene bridge. 2β,4aα,7,9β-Tetrahydroxy-1-methyl-8-methylenegibbane-1α,10β-dicarboxylic acid 1,4a-lactone exhibits a cyclic lactone ring, which contributes to its potential biological activities and applications.

Uses

Used in Plant Growth Regulation:
2β,4aα,7,9β-Tetrahydroxy-1-methyl-8-methylenegibbane-1α,10β-dicarboxylic acid 1,4a-lactone is used as a plant growth regulator for promoting the growth and elongation of plant cells. Its structural similarity to Gibberellic Acid, a known plant hormone, suggests that it may have similar physiological and morphological effects on plants, even at low concentrations.
Used in Pharmaceutical Industry:
Given its complex structure and multiple functional groups, 2β,4aα,7,9β-Tetrahydroxy-1-methyl-8-methylenegibbane-1α,10β-dicarboxylic acid 1,4a-lactone may be used as a starting material or intermediate in the synthesis of various pharmaceutical compounds. Its potential biological activities could be harnessed for the development of new drugs targeting specific diseases or conditions.
Used in Chemical Research:
The unique structure of 2β,4aα,7,9β-Tetrahydroxy-1-methyl-8-methylenegibbane-1α,10β-dicarboxylic acid 1,4a-lactone makes it an interesting subject for chemical research. It can be used as a model compound to study the properties and reactivity of similar diterpenoid compounds, contributing to the advancement of organic chemistry and the discovery of new synthetic methods or applications.
Used in Cosmetics Industry:
Due to its potential biological activities and the presence of hydroxyl groups, 2β,4aα,7,9β-Tetrahydroxy-1-methyl-8-methylenegibbane-1α,10β-dicarboxylic acid 1,4a-lactone may find applications in the cosmetics industry as an active ingredient in skincare or hair care products. It could be used for its potential moisturizing, anti-aging, or protective properties, depending on its specific effects on human skin and hair.
Used in Environmental Applications:
The compound's ability to interact with biopolymers and macromolecules may also make it suitable for environmental applications, such as in the development of biodegradable materials or as a component in environmental remediation processes. Further research would be needed to explore these potential uses and to determine the compound's effectiveness in such applications.

Check Digit Verification of cas no

The CAS Registry Mumber 105593-21-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,5,9 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105593-21:
(8*1)+(7*0)+(6*5)+(5*5)+(4*9)+(3*3)+(2*2)+(1*1)=113
113 % 10 = 3
So 105593-21-3 is a valid CAS Registry Number.

105593-21-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ent-3α,10β,13,15α-tetrahydroxy-20-norgibberell-16-ene-7,19-dioic acid 19,10-lactone

1.2 Other means of identification

Product number -
Other names Gibberellin A72

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:105593-21-3 SDS

105593-21-3Downstream Products

105593-21-3Relevant articles and documents

Partial Synthesis of the 15β-Hydroxygibberellins A67 and A68 and of 15β-hydroxygibberellinsb A1 and A3

Dolan, Simon C.,MacMillan, Jake

, p. 2741 - 2746 (2007/10/02)

The structures of two new higher plant gibberellins, A67 (7) and A68 (4), have been established by their partial synthesis from gibberellin A3 (2).In aadition, 15β-hydroxyGA1 (8) and 15β-hydroxyGA3 (3

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