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1,6-bis(1,3-benzodioxol-5-yl)hexane-1,6-dione is a complex organic compound with the molecular formula C18H14O6. It is characterized by a central hexane-1,6-dione backbone, which is flanked by two 1,3-benzodioxol-5-yl groups. The benzodioxol-5-yl groups are derived from benzene rings with two oxygen atoms forming a dioxole ring fused at the 1 and 3 positions. 1,6-bis(1,3-benzodioxol-5-yl)hexane-1,6-dione is known for its potential applications in the synthesis of various pharmaceuticals and other organic compounds due to its unique structure and reactivity. It is typically synthesized through a series of chemical reactions and is used as an intermediate in the preparation of more complex molecules. The compound's properties, such as its solubility and stability, can be influenced by the specific conditions under which it is synthesized and stored.

6268-56-0

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6268-56-0 Usage

General Description

1,6-bis(1,3-benzodioxol-5-yl)hexane-1,6-dione is a chemical compound with a complex molecular structure. It is a dione, meaning it contains two carbonyl groups, and it has hexane and benzodioxol groups in its structure. 1,6-bis(1,3-benzodioxol-5-yl)hexane-1,6-dione has potential applications in the field of organic chemistry as a building block for the synthesis of other molecules. It may also have potential pharmaceutical applications due to its unique structure and properties. However, as with any chemical compound, further research and testing would be necessary to fully understand its potential uses and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 6268-56-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,6 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6268-56:
(6*6)+(5*2)+(4*6)+(3*8)+(2*5)+(1*6)=110
110 % 10 = 0
So 6268-56-0 is a valid CAS Registry Number.

6268-56-0SDS

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 1,6-bis(1,3-benzodioxol-5-yl)hexane-1,6-dione

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

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More Details:6268-56-0 SDS

6268-56-0Relevant academic research and scientific papers

Lewis Acid-Promoted Disproportionation Reaction of Aromatic Vinyl Ethers and Acetals and Its Application to the Synthesis of Paracotoin

Gong, Young Dae,Tanaka, Hiroko,Iwasawa, Nobuharu,Narasaka, Koichi

, p. 2181 - 2185 (2007/10/03)

Aromatic vinyl ethers and acetals underwent a novel addition-fragmentation reaction affording olefins and esters in the presence of a Lewis acid. This reaction was applied to intramolecular cyclization reaction, giving five or six membered ring compounds in good yields. Paracotoin, an intermediate in the biosynthesis of shikimic acid, was synthesized using this cyclization reaction as the key step.

Synthesis and structure activity relationships of fibrinolytic 1,ω diphenyl 1,ω alkanediamines

Fliedner Jr,Myers,Schor,Pachter

, p. 749 - 754 (2007/10/06)

The promising results obtained in animal clot lysis experiments with the fibrinolytic bis(tetrahydroiso quinolines) VI prompted the preparation of a related series of 1,ω diphenyl 1,ω alkanediamines V. As measured in the standard rat screen (ip) the compo

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