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2,7-Benzodioxecin-1,8-dione,3,4,5,6-tetrahydro-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29246-20-6

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29246-20-6 Usage

Derivative of

2,7-benzodioxecin-1,4-dione

Ring Structure

Tetrahydrofuran ring

Properties

Anticancer: Exhibits potential in combating cancer cells.
Antiviral: Shows effectiveness against viruses.
Antioxidant: Capable of neutralizing harmful free radicals.
Anti-inflammatory: Reduces inflammation in biological systems.

Research Status

Ongoing studies to explore its therapeutic potential further and develop it into pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 29246-20-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,2,4 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 29246-20:
(7*2)+(6*9)+(5*2)+(4*4)+(3*6)+(2*2)+(1*0)=116
116 % 10 = 6
So 29246-20-6 is a valid CAS Registry Number.

29246-20-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4,5,6-tetrahydrobenzo[c][1,6]dioxecine-1,8-dione

1.2 Other means of identification

Product number -
Other names 3,4,5,6-Tetrahydro-2,7-benzodioxacyclodecen-1,8-dion

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:29246-20-6 SDS

29246-20-6Downstream Products

29246-20-6Relevant academic research and scientific papers

Silver carboxylate promoted lactonization: A general method applicable to prepare medium and large-sized lactones without high dilution or slow addition

Liu, Le,Xu, Shimin,Zhou, Hongwei

supporting information, p. 8386 - 8391 (2013/09/02)

Efficient and applicable approach to macrolactonizations, with ready availability of starting materials and simple operation, remains a challenging task for the organic community. We developed a 'freshman-can-do' protocol to medium- and large-sized lactones, not depending on high-dilution or slow addition techniques. Application of this method for the synthesis of natural lactones or potentially pharmaceutical compounds might be useful for organic chemists and pharmacists.

Microwave-assisted rutheniun-catalyzed olefin metathesis under solvent-free conditions

Thanh, Giang Vo,Loupy, Andre

, p. 9091 - 9094 (2007/10/03)

An efficient method for ring-closing metathesis under solvent-free conditions and by microwave activation was esteblished. Non-thermal microwave specific effects were evident.

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