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52157-62-7

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52157-62-7 Usage

Type of Compound

Organobromine compound

Structure

Thiophene ring with a bromine atom and a 1,3-dioxolan-2-yl substituent

Applications

Organic synthesis and pharmaceutical research

Potential Uses

Development of new drugs and materials

Reactivity

Ability to undergo various chemical reactions

Versatility

Serves as a building block in the synthesis of complex organic molecules

Check Digit Verification of cas no

The CAS Registry Mumber 52157-62-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,1,5 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 52157-62:
(7*5)+(6*2)+(5*1)+(4*5)+(3*7)+(2*6)+(1*2)=107
107 % 10 = 7
So 52157-62-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H7BrO2S/c8-6-2-1-5(11-6)7-9-3-4-10-7/h1-2,7H,3-4H2

52157-62-7SDS

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 2-(5-bromothiophen-2-yl)-1,3-dioxolane

1.2 Other means of identification

Product number -
Other names 1,3-Dioxolane,2-(5-bromo-2-thienyl)

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:52157-62-7 SDS

52157-62-7Relevant articles and documents

Structurally Diverse Poly(thienylene vinylene)s (PTVs) with Systematically Tunable Properties through Acyclic Diene Metathesis (ADMET) and Postpolymerization Modification

Zhang, Zhen,Qin, Yang

, p. 3318 - 3327 (2016)

Poly(thienylene vinylene)s (PTVs) are a unique class of low bandgap conjugated polymers that have received relatively little attention in organic electronic applications due to the limitations in conventional synthetic methodologies that are not capable to produce PTV structures beyond the rudimentary forms. We report here facile synthetic methods, combining acyclic diene metathesis (ADMET) and postpolymerization modification reactions, toward a series of structurally diverse PTVs. Specifically, halogen substituents including F, Cl, Br, and I, and conjugated thienyl groups bearing different substituents, have been installed onto every thiophene unit along the PTV backbones. While halogen substitution lowers both the HOMO and LUMO energy levels of the polymers, the overall optical properties are similar to the conventional unsubstituted PTVs. On the other hand, with increasing sizes of halogen atoms, the polymer crystallinity decreases caused by steric hindrance induced main-chain nonplanarity as suggested by density functional theory (DFT) calculations and confirmed by X-ray diffraction (XRD) and absorption measurements. With the cross-conjugated thienyl side-chains, the PTV polymers are all amorphous due to the large dihedral angles between the main-chain and side-chain thienyl rings. However, with strongly electron-withdrawing groups attached on the side-chain thiophene rings, new electronic transitions located at lower energies are observed, which have never been observed in PTVs and are assigned to main-chain to side-chain intramolecular charge transfer (ICTs) transitions. Such ICT transitions can potentially alter the PTV excited states ordering and dynamics, as evidenced by the appearance of fluorescence in one of the cross-conjugated PTVs bearing strong electron-withdrawing cyanoester vinylene groups. Applications of these new PTVs in bulk heterojunction (BHJ) organic solar cells (OSCs) have been attempted, and preliminary results showed much improved performances over devices using conventional PTVs, especially for those applying the cross-conjugated PTVs. Our methodologies are highly versatile in preparing PTVs with systematically varied structures that for the first time provide means to study and gain better understandings on the structure-property relationships of this unique class of materials and to potentially generate novel polymers tailor-designed for specific electronic applications.

THIOPHENE- SUB STITUED TETRACYCLIC COMPOUNDS AND METHODS OF USE THEREOF FOR THE TREATMENT OF VIRAL DISEASES

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Page/Page column 194, (2014/08/06)

Disclosed are novel Thiophene-Subsituted Tetracyclic Compounds of Formula (I). And pharmaceutically acceptable salts thereof, wherein A, A', R2, R3, R4 and R5 are as defined herein. The compositions comprising at least one Thiophene-Subsituted Tetracyclic Compounds, and methods of using the Thiophene-Subsituted Tetracyclic Compounds for treating or preventing HCV infection in a patient are also disclosed.

ANTI-INFLAMMATORY COMPOUND HAVING INHIBITORY ACTIVITY AGAINST MULTIPLE TYROSINE KINASES AND PHARMACEUTICAL COMPOSITION CONTAINING SAME

-

Paragraph 0261-0263, (2013/03/28)

The present invention is for the anti-inflammatory compounds that have an inhibitory activity against protein tyrosine kinases and their pharmaceutical composition(s) containing the compound as the active ingredient. Since the compounds of the present invention can inhibit multiple protein kinases associated with inflammatory diseases and immune disorders, they are useful for their prevention or treatment.

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