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162473-22-5

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162473-22-5 Usage

General Description

Subelliptene G is a chemical compound found in many essential oils, particularly in the oils of several Melaleuca species, such as Melaleuca leucadendra and Melaleuca linariifolia. It belongs to the class of chemical compounds known as oxygenated sesquiterpenoids and is characterized by its complex structure and strong, earthy aroma. Its potential therapeutic properties include anti-inflammatory, antimicrobial, and analgesic effects, making it a valuable ingredient in traditional medicine and aromatherapy. Studies have also shown that Subelliptene G may have potential as a natural remedy for various skin conditions and respiratory ailments, as well as for its ability to support overall well-being and relaxation.

Check Digit Verification of cas no

The CAS Registry Mumber 162473-22-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,4,7 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 162473-22:
(8*1)+(7*6)+(6*2)+(5*4)+(4*7)+(3*3)+(2*2)+(1*2)=125
125 % 10 = 5
So 162473-22-5 is a valid CAS Registry Number.

162473-22-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4,5-Trihydroxy-9H-xanthen-9-one

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:162473-22-5 SDS

162473-22-5Downstream Products

162473-22-5Relevant articles and documents

Construction of Highly Functionalized Xanthones via Rh-Catalyzed Cascade C-H Activation/ O-Annulation

Nale, Sagar D.,Maiti, Debabrata,Lee, Yong Rok

supporting information, p. 2465 - 2470 (2021/04/05)

A facile and efficient strategy for obtaining functionalized and multihydroxylated xanthones via Rh catalysis under redox-neutral conditions is developed. Diverse salicylaldehydes bearing heterocycles, aromatics, and fused aromatics can be rapidly coupled with 1,4-benzoquinones or 1,4-hydroquinones to afford valuable xanthones via cascade C-H/O-H functionalization and annulation. This protocol provides a rapid synthetic approach to obtain biologically active materials through late-stage functionalization and prepares natural products such as subelliptenone, pruniflorone N, and ravenelin.

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