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6314-28-9

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6314-28-9 Usage

Chemical Properties

off-white to yellowish-beige crystalline powder

Uses

Thianaphthene-2-carboxylic acid may be used for the fabrication of carboxylated conducting polymer/CNTs (carbon nanotubes) composites thin films.

Synthesis Reference(s)

The Journal of Organic Chemistry, 21, p. 39, 1956 DOI: 10.1021/jo01107a007

General Description

Thianaphthene-2-carboxylic acid, a benzothiophene, is a heterocyclic sulfur compound. It undergoes degradation (23%) by employing a mixture of washed cells of Rhodococcus erythropolis DS-3 and Gordonia sp. C-6.

Check Digit Verification of cas no

The CAS Registry Mumber 6314-28-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6314-28:
(6*6)+(5*3)+(4*1)+(3*4)+(2*2)+(1*8)=79
79 % 10 = 9
So 6314-28-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H6O2S/c10-9(11)8-5-6-3-1-2-4-7(6)12-8/h1-5H,(H,10,11)/p-1

6314-28-9 Well-known Company Product Price

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  • Alfa Aesar

  • (A12471)  Benzo[b]thiophene-2-carboxylic acid, 98%   

  • 6314-28-9

  • 1g

  • 257.0CNY

  • Detail
  • Alfa Aesar

  • (A12471)  Benzo[b]thiophene-2-carboxylic acid, 98%   

  • 6314-28-9

  • 5g

  • 982.0CNY

  • Detail
  • Alfa Aesar

  • (A12471)  Benzo[b]thiophene-2-carboxylic acid, 98%   

  • 6314-28-9

  • 25g

  • 4167.0CNY

  • Detail
  • Aldrich

  • (467464)  Thianaphthene-2-carboxylicacid  98%

  • 6314-28-9

  • 467464-5G

  • 960.57CNY

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6314-28-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Thianaphthene-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names Benzo[b]thiophene-2-carboxylic acid

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:6314-28-9 SDS

6314-28-9Relevant articles and documents

-

Shirley,Cameron

, p. 2788 (1950)

-

Milled Dry Ice as a C1 Source for the Carboxylation of Aryl Halides

O'Brien, Connor J.,Nicewicz, David A.

supporting information, p. 814 - 816 (2021/03/01)

The use of carbon dioxide as a C1 chemical feedstock remains an active field of research. Here we showcase the use of milled dry ice as a method to promote the availability of CO 2in a reaction solution, permitting practical synthesis of arylcarboxylic acids. Notably, the use of milled dry ice produces marked increases in yields relative to those obtained with gaseous CO 2, as previously reported in the literature.

Photo-induced deep aerobic oxidation of alkyl aromatics

Wang, Chang-Cheng,Zhang, Guo-Xiang,Zuo, Zhi-Wei,Zeng, Rong,Zhai, Dan-Dan,Liu, Feng,Shi, Zhang-Jie

, p. 1487 - 1492 (2021/07/10)

Oxidation is a major chemical process to produce oxygenated chemicals in both nature and the chemical industry. Presently, the industrial manufacture of benzoic acids and benzene polycarboxylic acids (BPCAs) is mainly based on the deep oxidation of polyalkyl benzene, which is somewhat suffering from environmental and economical disadvantage due to the formation of ozone-depleting MeBr and corrosion hazards of production equipment. In this report, photo-induced deep aerobic oxidation of (poly)alkyl benzene to benzene (poly)carboxylic acids was developed. CeCl3 was proved to be an efficient HAT (hydrogen atom transfer) catalyst in the presence of alcohol as both hydrogen and electron shuttle. Dioxygen (O2) was found as a sole terminal oxidant. In most cases, pure products were easily isolated by simple filtration, implying large-scale implementation advantages. The reaction provides an ideal protocol to produce valuable fine chemicals from naturally abundant petroleum feedstocks. [Figure not available: see fulltext.].

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