2H-Pyran, 2-[(1-ethynylhexyl)oxy]tetrahydro-

Base Information

• Chemical Name: 2H-Pyran, 2-[(1-ethynylhexyl)oxy]tetrahydro-
• CAS No.: 834-16-2
• Molecular Formula: C₁₃H₂₂O₂
• Molecular Weight: 210.316
• DSSTox Substance ID: DTXSID30472690
• Nikkaji Number: J1.039.692A

Synonyms:834-16-2;2H-Pyran, 2-[(1-ethynylhexyl)oxy]tetrahydro-;SCHEMBL3849576;DTXSID30472690;IKSVRFLFLHXCFK-UHFFFAOYSA-N;3-(2-tetrahydropyranyloxy)-1-octyne;2-(1-ethynyl-hexyloxy)tetrahydropyran;3-(tetrahydropyran-2-yloxy)-1-octyne;2-(oct-1-yn-3-yloxy)tetrahydro-2H-pyran;3(RS)-(tetrahydropyran-2-yl)oxy-1-octyne

Chemical Property of 2H-Pyran, 2-[(1-ethynylhexyl)oxy]tetrahydro-

Chemical Property:

• XLogP3: 3.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 6
• Exact Mass: 210.161979940
• Heavy Atom Count: 15
• Complexity: 204

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCC(C#C)OC1CCCCO1

Refernces

Thieno<2,3-c>pyrroles: Synthesis, Diels-ALder Reaction, and Synthetic Utility

10.1021/jo00295a038

The research focuses on the synthesis and chemical reactions of thieno[2,3-c]pyrroles. The authors developed a novel method for synthesizing these compounds through a retro-malonate addition reaction, starting from 3-methyl-2-thiophenecarboxaldehyde and diethyl malonate. They also explored the Diels-Alder reactions of thieno[2,3-c]pyrroles with reactive dienophiles such as N-phenylmaleimide and dimethyl acetylenedicarboxylate, leading to the formation of cycloadducts. The study includes the synthesis of various N-substituted thieno[2,3-c]pyrroles and their subsequent reactions to produce compounds like benzo[b]thiophene. The research also investigates the free-energy barriers of inversion of the imine nitrogens in the cycloadducts using variable-temperature 'H NMR spectroscopy. The study provides valuable insights into the synthetic utility and reactivity of thieno[2,3-c]pyrroles, contributing to the field of organic chemistry and potentially to the development of new pharmaceuticals and electroconducting polymers.

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