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naphtho[1,8-de][1,3]dithiine

Base Information
  • Chemical Name:naphtho[1,8-de][1,3]dithiine
  • CAS No.:204-14-8
  • Molecular Formula:C11H8S2
  • Molecular Weight:204.317
  • Hs Code.:
naphtho[1,8-de][1,3]dithiine

Synonyms:Naphtho[1,8-de]-m-dithiin(8CI)

Suppliers and Price of naphtho[1,8-de][1,3]dithiine
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
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  • price
Total 5 raw suppliers
Chemical Property of naphtho[1,8-de][1,3]dithiine
Chemical Property:
  • Vapor Pressure:4.37E-06mmHg at 25°C 
  • Boiling Point:394.8oC at 760 mmHg 
  • Flash Point:212.2oC 
  • Density:1.347g/cm3 
Purity/Quality:

99% *data from raw suppliers

Safty Information:
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  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of naphtho[1,8-de][1,3]dithiine

There total 1 articles about naphtho[1,8-de][1,3]dithiine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With sodium hydride; In tetrahydrofuran; Ambient temperature;
DOI:10.1246/cl.1986.551
upstream raw materials:

diiodomethane

naphthalene-1,8-dithiol

Refernces

Donor-Acceptor-Acceptor 1,3-Bisdiazo Compounds: An Exploration of Synthesis and Stepwise Reactivity

10.1021/acs.orglett.0c00103

The study focuses on the synthesis and reactivity of a unique class of acyclic, bis-diazo compounds known as donor-acceptor-acceptor 1,3-bisdiazo compounds, which are derived from acyclic β-keto esters and are highly reactive at the donor-acceptor diazo unit. These compounds were used to explore their potential in C?H functionalization, a technology that allows carbon?hydrogen bonds to be transformed into diverse functionalities and new carbon?carbon bonds. The purpose of using these chemicals was to investigate their capacity for performing a variety of transformations, particularly in the context of dirhodium-catalyzed carbene C?H insertions, which are valuable for synthetic applications. The study also aimed to understand the reactivity of these compounds, especially their ability to undergo stepwise diazo decompositions and participate in sequential carbene transformations. Key chemicals used in the study include rhodium acetate, various alcohols, and acyclic β-keto esters, which served as starting materials and reagents in the synthesis and reactivity experiments.

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