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5650-52-2

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5650-52-2 Usage

General Description

4,5-Dihydrocyclopenta[b]thiophen-6-one, also known as tetrahydrothiophenone, is a chemical compound with a molecular formula C6H8OS. It is a cyclic ketone with a five-membered ring containing a sulfur atom. 4,5-Dihydrocyclopenta[b]thiophen-6-one is commonly used as a chemical intermediate in the synthesis of pharmaceuticals, agrochemicals, and fragrances. Its unique structure and reactivity make it a valuable building block in organic synthesis. Additionally, 4,5-Dihydrocyclopenta[b]thiophen-6-one is also used as a flavoring agent in food products. The compound's diverse range of applications and its ability to easily undergo chemical reactions make it a versatile and important compound in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 5650-52-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,5 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5650-52:
(6*5)+(5*6)+(4*5)+(3*0)+(2*5)+(1*2)=92
92 % 10 = 2
So 5650-52-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H6OS/c8-6-2-1-5-3-4-9-7(5)6/h3-4H,1-2H2

5650-52-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4H-Cyclopenta[b]thiophen-6(5H)-one

1.2 Other means of identification

Product number -
Other names 4,5-Dihydrocyclopenta[b]thiophen-6-one

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:5650-52-2 SDS

5650-52-2Relevant articles and documents

Control of the Bandgap of Conducting Polymers by Rigidification of the ?-Conjugated System

Roncali, Jean,Thobie-Gautier, Christine,Elandaloussi, El Hadj,Frere, Pierre

, p. 2249 - 2250 (1994)

Rigidification of E-1,2(2,2'-dithienylethylene) by bridging the thiophene rings with the central double bond leads to a ca. 0.40 eV decrease of the bandgap of the resulting conducting polymer.

SPIROCYCLIC HAT INHIBITORS AND METHODS FOR THEIR USE

-

, (2016/04/10)

Compounds having a structure of Formula (IX) or a stereoisomer, tautomer or pharmaceutically acceptable salt thereof, wherein R1, R2a, R2b, R3a, R3b, R4a, R4b, Q1----Q2, R6, R7, A, B, W, x, and y are as defined herein and are provided. Pharmaceutical compositions comprising such compounds and methods for treating various HAT-related conditions or diseases, including cancer, by administration of such compounds are also provided.

Fused thiophene-based conjugated polymers and their use in optoelectronic devices

-

, (2015/11/27)

The present teachings relate to certain polymeric compounds and their use as organic semiconductors in organic and hybrid optical, optoelectronic, and/or electronic devices such as photovoltaic cells, light emitting diodes, light emitting transistors, and field effect transistors. The disclosed compounds can provide improved device performance, for example, as measured by power conversion efficiency, fill factor, open circuit voltage, field-effect mobility, on/off current ratios, and/or air stability when used in photovoltaic cells or transistors. The disclosed compounds can have good solubility in common solvents enabling device fabrication via solution processes.

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