Welcome to LookChem.com Sign In|Join Free

CAS

  • or

17249-80-8

Post Buying Request

17249-80-8 Suppliers

Recommended suppliersmore

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

17249-80-8 Usage

Chemical Properties

clear colorless to light yellow liquid

Uses

3-Chlorothiophene was used in the synthesis of poly(3-chlorothiophene) films by direct oxidation in mixed electrolytes of boron trifluoride diethyl etherate and trifluroacetic acid.

Synthesis Reference(s)

Journal of Heterocyclic Chemistry, 14, p. 281, 1977 DOI: 10.1002/jhet.5570140224

General Description

Electrochemical homopolymerization of 3-chlorothiophene and copolymerization with 3-methylthiophene in ionic liquid has been investigated by potentiodynamic and galvanostat methods.

Check Digit Verification of cas no

The CAS Registry Mumber 17249-80-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,4 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17249-80:
(7*1)+(6*7)+(5*2)+(4*4)+(3*9)+(2*8)+(1*0)=118
118 % 10 = 8
So 17249-80-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H3ClS/c5-4-1-2-6-3-4/h1-3H

17249-80-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (C1192)  3-Chlorothiophene  >97.0%(GC)

  • 17249-80-8

  • 5g

  • 590.00CNY

  • Detail
  • TCI America

  • (C1192)  3-Chlorothiophene  >97.0%(GC)

  • 17249-80-8

  • 25g

  • 1,950.00CNY

  • Detail
  • Alfa Aesar

  • (B22669)  3-Chlorothiophene, 98%, may contain up to 2% DMF   

  • 17249-80-8

  • 5g

  • 490.0CNY

  • Detail
  • Alfa Aesar

  • (B22669)  3-Chlorothiophene, 98%, may contain up to 2% DMF   

  • 17249-80-8

  • 25g

  • 1562.0CNY

  • Detail
  • Alfa Aesar

  • (B22669)  3-Chlorothiophene, 98%, may contain up to 2% DMF   

  • 17249-80-8

  • 100g

  • 6171.0CNY

  • Detail
  • Aldrich

  • (341061)  3-Chlorothiophene  98%

  • 17249-80-8

  • 341061-5G

  • 586.17CNY

  • Detail

17249-80-8SDS

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 3-Chlorothiophene

1.2 Other means of identification

Product number -
Other names 3-CHLOROTHIOPHENE

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:17249-80-8 SDS

17249-80-8Related news

Probing the adsorption structure of a multifunctional organic molecule: a NIXSW and NEXAFS study of 3-CHLOROTHIOPHENE (cas 17249-80-8) on Cu(111)08/30/2019

The adsorption structure of 3-chlorothiophene on Cu(111) has been investigated using a combination of normal incidence X-ray standing wavefield absorption (NIXSW) and near edge X-ray absorption fine structure (NEXAFS) spectroscopy. For coverages up to saturation of the chemisorbed layer, the 3-c...detailed

Low potential electrochemical polymerization of 3-CHLOROTHIOPHENE (cas 17249-80-8) in mixed electrolytes of boron trifluoride diethyl etherate and trifluoroacetic acid08/25/2019

Poly(3-chlorothiophene) (PCT) films were synthesized electrochemically by direct oxidation of 3-chlorothiophene (CT) in mixed electrolytes of boron trifluoride diethyl etherate (BFEE) and trifluroacetic acid (TFA). The oxidation potential of 3-chlorothiophene in pure BFEE was measured to be only...detailed

17249-80-8Relevant articles and documents

-

Perevalova et al.

, (1978)

-

Competitive reactivities of vinylthiyl radicals thermally generated from haloethylenes and hydrogen sulfide

Deryagina,Sukhomazova,Levanova

, p. 662 - 666 (2007/10/03)

Acetylene and its derivatives have been used for the first time as "traps" for vinylthiyl radicals generated in situ from hydrogen sulfide and haloethylenes in gas-phase processes. The competitive reactivity of the vinylthiyl radicals has been studied at 500-570 °C in the presence of two chemical "traps." The efficiency of chemical "traps" for the vinylthiyl radicals decreases in the following sequence: HC≡CPh > HC≡CH > MeC≡CH > CH2=CHCl. Acetylene is a more efficient "trap" for the vinylthiyl radicals than 1,2-dichloroethylene, from which they have been generated. The β-phenylvinylthiyl radicals generated during cothermolysis of halostyrene-hydrogen sulfide-acetylene component ternary systems undergo first of all intramolecular ring closure to give benzothiophene, which is a thermodynamically favorable system; the reaction of these radicals with acetylene and its derivatives occurs much more slowly than heterocyclization. Phenylacetylene is a more efficient "trap" than acetylene. α-Phenylvinylthiyl radicals mostly react with acetylene to yield 2-phenylthiophene.

Herstellung von β-Halogenthiophenen durch Isomerisierung von α-Halogenthiophenen an Zeolithkatalysatoren

Dettmeier, Udo,Eichler, Klaus,Kuehlein, Klaus,Leupold, Ernst Ingo,Litterer, Heinz

, p. 470 - 471 (2007/10/02)

-

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

What can I do for you?
Get Best Price

Get Best Price for 17249-80-8