Welcome to LookChem.com Sign In|Join Free
  • or
1,2-bis(4-ethoxyphenyl)ethyne, also known as diethyl 4-ethynylbiphenyl-4,4'-dicarboxylate, is an organic compound characterized by a unique structure that features an ethynyl (acetylene) group connecting two 4-ethoxyphenyl rings. This molecule is notable for its rigid and planar structure, which can be useful in the design of materials with specific optical or electronic properties. It is a colorless solid that is insoluble in water but soluble in organic solvents. The compound is synthesized through the coupling of 4-ethoxyphenylmagnesium bromide with 4-iodoanisole, followed by a Sonogashira coupling reaction. 1,2-bis(4-ethoxyphenyl)ethyne is a precursor in the synthesis of various conjugated polymers and materials used in organic electronics, such as organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs), due to its ability to contribute to the formation of extended π-conjugated systems.

2132-63-0

Post Buying Request

2132-63-0 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

2132-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2132-63-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,3 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2132-63:
(6*2)+(5*1)+(4*3)+(3*2)+(2*6)+(1*3)=50
50 % 10 = 0
So 2132-63-0 is a valid CAS Registry Number.

2132-63-0Relevant academic research and scientific papers

Synthesis of Diarylethynes from Aryldiazonium Salts by Using Calcium Carbide as an Alkyne Source in a Deep Eutectic Solvent

Ma, Xiaolong,Li, Zheng

supporting information, p. 631 - 635 (2020/12/28)

An efficient method for the synthesis of diarylethynes from aryldiazonium salts by using calcium carbide as an alkyne source at room temperature in a deep eutectic solvent is described. The salient features of this protocol are an inexpensive and easy-to-handle alkyne source, a nonvolatile and recyclable solvent, mild conditions, and a simple workup procedure.

Palladium-Catalyzed Domino Alkenylation/Amination/Pyridination Reactions of 2-Vinylanilines with Alkynes: Access to Cyclopentaquinolines

Li, Dejun,Zeng, Fanlong

supporting information, p. 6498 - 6501 (2017/12/26)

A novel domino oxidative annulation of 2-vinylanilines with internal alkynes was developed to constitute a rare class of cyclopentaquinoline derivatives. This transformation encompasses four σ bonds formation, one quaternary carbon center construction, and pyridination steps in one pot under identical conditions, which fascinatingly increases the molecular complexity from easily available starting materials.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 2132-63-0