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"3,4,8,9-tetradehydro-2,5,7,10-tetrahydro-1,6-dioxecine" is a complex organic compound with a unique molecular structure. It is characterized by the presence of four hydrogen atoms removed from the 3, 4, 8, and 9 positions, and four hydrogen atoms added to the 2, 5, 7, and 10 positions, relative to a hypothetical parent compound. The term "dioxecine" in its name suggests the presence of two ether groups (oxygen atoms bonded to two carbon atoms) and a six-membered ring structure. 3,4,8,9-tetradehydro-2,5,7,10-tetrahydro-1,6-dioxecine is likely to be of interest in the field of organic chemistry, potentially for its reactivity, stability, or as a building block in the synthesis of more complex molecules. However, without additional context or specific applications, it's challenging to provide a more detailed summary of its properties or uses.

6573-64-4

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6573-64-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6573-64-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,7 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6573-64:
(6*6)+(5*5)+(4*7)+(3*3)+(2*6)+(1*4)=114
114 % 10 = 4
So 6573-64-4 is a valid CAS Registry Number.

6573-64-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,6-dioxacyclodeca-3,8-diyne

1.2 Other means of identification

Product number -
Other names 1,6-dioxa-cyclodeca-3,8-diyne

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:6573-64-4 SDS

6573-64-4Downstream Products

6573-64-4Relevant academic research and scientific papers

Double cationic propargylation: From linear to polycyclic ethers

Diaz, David,Martin, Tomas,Martin, Victor S.

, p. 3289 - 3291 (2007/10/03)

Equation presented The trapping of cations generated from Co2(CO)6-bispropargylic alcohols provided diethers in good yield. The procedure is also valid when two vicinal acetylenes are present. The methodology can be applied to the sy

Synthesis of Heterocyclic Diynes and their Reaction with CpCo(CO)2

Gleiter, Rolf,Rittinger, Stefan,Langer, Heinrich

, p. 357 - 363 (2007/10/02)

The preparation of the heterocyclic diynes 1,16-dithia-3,8-cyclodecadiyne (1b), thia-3,8-cyclodecadiyne (11), 1-thia-6-selena-3,8-cyclodecadiyne (12), oxa-3,8-cyclodecadiyne (13), 1,6-dioxa-3,8-cyclodecadiyne (14), 1-oxa-6-thia-3,8-cyclodecadiyne (15), 1,6-diselena-3,8-cyclodecadiyne (26), thia-3,9-cycloundecadiyne (22a), thia-3,13-cyclopentadecadiyne (22b) and its selena analogues 23a, 23b is described.The thia and monoselena compounds are obtained by a thia- or selenacyclization of the corresponding dibromides.Compound 26 has been obtained by a Misumi coupling reaction.The thiacycloalkadienes of medium-sized rings (10, 11) react with CpCo(CO)2 to yield (2,5)thiophenophane derivatives.Acyclic thiadialkynes or thiacyclodialkynes of larger ring size (22b) with CpCo(CO)2 by cycloaddition.

SYNTHESIS AND PROPERTIES OF TEN-MEMBERED CYCLODIYNES WITH ONE OR TWO HETERO ATOMS

Gleiter, Rolf,Rittinger, Stefan

, p. 4529 - 4532 (2007/10/02)

The synthesis of the heterocyclic decadiynes 1 and 2 via a cyclization sequence and subsequent CpCo-induced oligomerization of 1a as well as its acyclic analogues 3c and 9 are reported.

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