115227-74-2

Usage

10-membered ring

The compound has a ring structure with 10 atoms.

Sulfur atom

The compound contains a single sulfur atom as part of its structure.

Carbon-carbon triple bonds

The compound has two triple bonds between carbon atoms.

Organic compound

It is a compound that contains carbon atoms.

Polyacetylene

It belongs to a group of compounds with multiple carbon-carbon triple bonds.

Increased stability

The presence of the sulfur atom increases the stability of the compound.

Altered reactivity

The presence of the sulfur atom changes the reactivity of the compound.

Potential uses in organic synthesis

The compound can be used as a building block in the synthesis of other organic compounds.

Potential uses in materials science

The unique structure and properties of the compound may make it useful in the development of new materials.

Further research may uncover new uses

Ongoing research into the properties and applications of 1-thiacyclodeca-3,8-diyne may lead to the discovery of new and exciting uses for this chemical compound.

InChI:InChI=1/C9H10S/c1-2-4-6-8-10-9-7-5-3-1/h1-3,8-9H2

Upstream product

• 81077-35-2 nona-2,7-diyne-1,9-diol 
• 2396-63-6 hepta-1,6-diyne 
• 81077-34-1 C₁₉H₂₈O₄ 
• 115227-67-3 1,9-dibromo-2,7-nonadiyne 

Relevant academic research and scientific papers

Design, synthesis, and study of simple monocyclic conjugated enediynes. The 10-membered ring enediyne moiety of the enediyne anticancer antibiotics

Following the discovery of the enediyne anticancer antibiotics, investigations were initiated directed toward the design, synthesis, and study of simple monocyclic conjugated enediynes. In this article the synthesis of the parent 10-membered ring enediyne

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

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

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.