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6808-14-6

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6808-14-6 Usage

Description

(25R)-Furosta-5,20(22)-diene-3β,26-diol is a steroidal compound with a furostane skeleton, belonging to the class of sapogenins, which are natural steroid precursors found in various plants. This chemical possesses potential medicinal properties and is being explored for its potential use in pharmaceuticals due to its associated range of biological activities, including anti-inflammatory, immunomodulatory, and anticancer effects. Furthermore, it has been investigated for its potential to lower cholesterol levels and improve cardiovascular health, making it a promising compound with potential therapeutic applications.

Uses

Used in Pharmaceutical Industry:
(25R)-Furosta-5,20(22)-diene-3β,26-diol is used as a pharmaceutical precursor for the development of new drugs, leveraging its anti-inflammatory, immunomodulatory, and anticancer properties. Its potential to lower cholesterol levels and improve cardiovascular health also makes it a candidate for the treatment of related conditions.
Used in Nutraceutical Industry:
As a natural steroid precursor, (25R)-Furosta-5,20(22)-diene-3β,26-diol can be used as an ingredient in nutraceutical products aimed at promoting overall health and well-being, particularly in the areas of inflammation management and cardiovascular health.
Used in Cosmetic Industry:
Due to its potential anti-inflammatory and immunomodulatory effects, (25R)-Furosta-5,20(22)-diene-3β,26-diol may be utilized in cosmetic products designed to improve skin health and address issues related to inflammation and immune response in the skin.
Used in Research and Development:
(25R)-Furosta-5,20(22)-diene-3β,26-diol serves as a valuable compound in research and development for the discovery of new therapeutic agents and understanding its full range of biological activities, which could lead to novel applications in medicine and healthcare.

Check Digit Verification of cas no

The CAS Registry Mumber 6808-14-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,0 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6808-14:
(6*6)+(5*8)+(4*0)+(3*8)+(2*1)+(1*4)=106
106 % 10 = 6
So 6808-14-6 is a valid CAS Registry Number.

6808-14-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name η-diosgenin

1.2 Other means of identification

Product number -
Other names Pseudodiosgenin

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:6808-14-6 SDS

6808-14-6Relevant articles and documents

Synthesis and cytotoxic effect of pseudodiosgenyl saponins with thio-ring F

Zan, Xin,Gao, Jian,Gu, Guofeng,Liu, Shanshan,Sun, Bin,Liu, Lei,Lou, Hong-Xiang

supporting information, p. 1600 - 1604 (2014/03/21)

Both the sugar moieties and aglycons of steroid saponins play important roles for their bioactivities. In order to test the biological contribution of the glycosyl residue and search new saponins with notable anticancer activity, mono- and di-saccharide p

KHSO4-SiO2-MeOH An efficient selective solid-supported system for deprotection of alcohols from esters

Goswami, Amrit,Das, Ram N.,Borthakur, Naleen

, p. 1893 - 1895 (2008/09/19)

KHSO4-SiO2 can efficiently deprotect alcohols from esters through transesterification in methanol under mild condition. Esters of aromatic alcohols are easily transesterified at room temperature compared to the corresponding aliphatic or alicyclic alcohol. NAcetyl compounds and ethers are resistant to the reagent under the above condition. The method is very useful for preparation of biodiesel methyl ricinoleate from castor oil.

Studies on the coloration mechanism of furostanol derivatives with Ehrlich reagents. I. On the reaction of 3,26-dimethoxy-furost-5,20-diene with Ehrlich reagent

Konishi,Kiyosawa,Shoji

, p. 2111 - 2116 (2007/10/02)

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