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1015071-22-3

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1015071-22-3 Usage

General Description

5-Fluoro-2,3-thiophenedicarboxaldehyde is a chemical compound with the molecular formula C6H3FO3S. It is an aldehyde derivative of thiophene containing a fluorine atom. This chemical is primarily used in pharmaceutical and organic synthesis as a building block for various compounds. It is also known for its potential use as an intermediate in the development of new materials and drugs. Additionally, 5-Fluoro-2,3-thiophenedicarboxaldehyde is considered to have interesting properties that make it an important target for chemical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 1015071-22-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,5,0,7 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1015071-22:
(9*1)+(8*0)+(7*1)+(6*5)+(5*0)+(4*7)+(3*1)+(2*2)+(1*2)=83
83 % 10 = 3
So 1015071-22-3 is a valid CAS Registry Number.
InChI:InChI=1S/C6H3FO2S/c7-6-1-4(2-8)5(3-9)10-6/h1-3H

1015071-22-3 Well-known Company Product Price

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  • Aldrich

  • (708283)  5-Fluoro-2,3-thiophenedicarboxaldehyde  97%

  • 1015071-22-3

  • 708283-500MG

  • 2,543.58CNY

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1015071-22-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-fluorothiophene-2,3-dicarbaldehyde

1.2 Other means of identification

Product number -
Other names 5-Fluoro-2,3-thiophenedicarboxaldehyde

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:1015071-22-3 SDS

1015071-22-3Upstream product

1015071-22-3Relevant articles and documents

Chromophore fluorination enhances crystallization and stability of soluble anthradithiophene semiconductors

Subramanian, Sankar,Sung, Kyu Park,Parkin, Sean R.,Podzorov, Vitaly,Jackson, Thomas N.,Anthony, John E.

, p. 2706 - 2707 (2008/09/19)

We report dramatic improvements in the stability and crystallinity arising from partial fluorination of soluble anthradithiophene derivatives. These fluorinated materials still behave as p-type semiconductors but with dramatic increases in thermal and photostability compared to the non-fluorinated derivatives. The triethylsilyl-substituted material forms highly crystalline films even from spin-cast solutions, leading to devices with maximum hole mobility greater than1.0 cm2/V s. In contrast, the triisopropylsilyl derivative forms large, high-quality crystals that could serve as the substrate for transistor fabrication. For this compound, mobility as high as 0.1 cm2/V s was measured on the free-standing crystal. Copyright

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