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1,4-Di(2-thienyl)-1,3-butadiene is a distinctive organosulfur compound, primarily composed of carbon, hydrogen, and sulfur. It features a butadiene core with two thiophene rings attached, which may contribute to its potential applications in the realms of organic, polymer, and materials chemistry. Despite its intriguing structure, there is a scarcity of detailed information regarding its properties, toxicity, and its role in commercial products or industrial processes. Further research is necessary to explore its practical applications and to assess any potential health or environmental risks.

23354-93-0

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23354-93-0 Usage

Uses

Used in Organic Chemistry:
1,4-Di(2-thienyl)-1,3-butadiene is used as a building block for the synthesis of various organic compounds due to its unique structure that combines a butadiene core with two thiophene rings.
Used in Polymer Chemistry:
1,4-Di(2-thienyl)-1,3-butadiene is used as a monomer in the development of new polymers, potentially offering novel properties and applications in materials science.
Used in Materials Chemistry:
1,4-Di(2-thienyl)-1,3-butadiene is used as a component in the creation of advanced materials, with its chemical structure potentially contributing to the development of materials with enhanced properties for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 23354-93-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,3,5 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 23354-93:
(7*2)+(6*3)+(5*3)+(4*5)+(3*4)+(2*9)+(1*3)=100
100 % 10 = 0
So 23354-93-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H10S2/c1(5-11-7-3-9-13-11)2-6-12-8-4-10-14-12/h1-10H/b5-1+,6-2+

23354-93-0 Well-known Company Product Price

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  • TCI America

  • (D2077)  1,4-Di(2-thienyl)-1,3-butadiene (mixture of isomers)  >97.0%(GC)

  • 23354-93-0

  • 1g

  • 990.00CNY

  • Detail
  • TCI America

  • (D2077)  1,4-Di(2-thienyl)-1,3-butadiene (mixture of isomers)  >97.0%(GC)

  • 23354-93-0

  • 5g

  • 3,450.00CNY

  • Detail

23354-93-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-thiophen-2-ylbuta-1,3-dienyl)thiophene

1.2 Other means of identification

Product number -
Other names 1,4-DI(2-THIENYL)-1,3-BUTADIENE

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:23354-93-0 SDS

23354-93-0Downstream Products

23354-93-0Relevant academic research and scientific papers

Reactivity differences between 2,4- and 2,5-disubstituted zirconacyclopentadienes: A highly selective and general approach to 2,4-disubstituted phospholes

Bousrez, Guillaume,Jaroschik, Florian,Martinez, Agathe,Harakat, Dominique,Nicolas, Emmanuel,Le Goff, Xavier F.,Szymoniak, Jan

supporting information, p. 10997 - 11004 (2013/09/12)

Mixtures of 2,4- and 2,5-disubstituted zirconacyclopentadienes were obtained by the reductive dimerisation of terminal alkynes using the Cp 2ZrCl2/lanthanum system. Reactions of dihalophosphines with these mixtures afforded selectively the corresponding 2,4-disubstituted phospholes and 1,4-disubstituted butadienes. A new series of phospholes was characterized by multi-nuclear NMR spectroscopy and X-ray analysis. A possible explanation for the observed selectivity was obtained from X-ray studies and DFT analysis of the intermediate zirconacyclopentadienes. The Royal Society of Chemistry 2013.

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