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115753-79-2

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115753-79-2 Usage

General Description

Galanolactone is a chemical compound derived from the plant species of the ginger family, typically found in East Asia. It is known for its pharmacological properties and is primarily used in many traditional medicines for its numerous health benefits. It has been found to exhibit anti-allergic, anti-inflammatory, anticancer, and antioxidant effects. Moreover, it has antifungal, antiviral, and antimicrobial qualities which contribute to overall health and wellness. Galanolactone has also demonstrated abilities to protect the liver, as well as potential in treating anxiety without causing sedation.

Check Digit Verification of cas no

The CAS Registry Mumber 115753-79-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,7,5 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 115753-79:
(8*1)+(7*1)+(6*5)+(5*7)+(4*5)+(3*3)+(2*7)+(1*9)=132
132 % 10 = 2
So 115753-79-2 is a valid CAS Registry Number.
InChI:InChI=1/C20H30O3/c1-18(2)9-4-10-19(3)15(18)7-11-20(13-23-20)16(19)6-5-14-8-12-22-17(14)21/h5,15-16H,4,6-13H2,1-3H3/b14-5+/t15-,16+,19-,20?/m0/s1

115753-79-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Galanolactone

1.2 Other means of identification

Product number -
Other names -

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:115753-79-2 SDS

115753-79-2Downstream Products

115753-79-2Relevant articles and documents

Conversion of sclareol into (+)-galanolactone and (+)-labdienedial

Jung, Mankil,Lee, Seokjoon,Yoon, Byunghee

, p. 2871 - 2874 (1997)

A short, regiospecific and first synthesis of (+)-galanolactone 5 and (+)-labdienedial 11 was achieved from sclareol, respectively.

Total synthesis of (±)-galanoctone

Herlem,Kervagoret,Khuong-Huu

, p. 553 - 556 (2007/10/02)

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