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2-Bromobenzothiophene sulfone is an organic chemical compound characterized by its molecular formula C8H5BrOS2. It is a derivative of benzothiophene, which is a heterocyclic compound consisting of a benzene ring fused to a thiophene ring. The presence of a bromine atom at the 2-position and a sulfone group (-SO2) attached to the thiophene ring gives 2-Bromobenzothiophene sulfone unique chemical properties. It is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its reactivity and structural diversity. The compound is typically synthesized through bromination and sulfonation reactions and is known for its stability and potential applications in the development of new chemical entities.

5350-05-0

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5350-05-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5350-05-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,5 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5350-05:
(6*5)+(5*3)+(4*5)+(3*0)+(2*0)+(1*5)=70
70 % 10 = 0
So 5350-05-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H5BrO2S/c9-8-5-6-3-1-2-4-7(6)12(8,10)11/h1-5H

5350-05-0SDS

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-bromo-1-benzothiophene 1,1-dioxide

1.2 Other means of identification

Product number -
Other names 2-Brom-thianaphthen-1,1-dioxid

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:5350-05-0 SDS

5350-05-0Relevant academic research and scientific papers

Photomechanical Luminescence from Through-Space Conjugated AIEgens

Fan, Jianzhong,Guo, Jingjing,Liu, Xinzhi,Tang, Ben Zhong,Zhao, Zujin

supporting information, p. 8828 - 8832 (2020/03/04)

Transforming molecular motions into the macroscopic scale is a topic of great interest to nanoscience. The photomechanical effect is a promising strategy to achieve this goal. Herein, we report an intriguing photomechanical luminescence driven by the photodimerization of 2-phenylbenzo[b]thiophene 1,1-dioxide (P-BTO) in molecular crystals and elucidate the working mechanism and substituent effect through crystallographic analysis and theoretical calculations. Striking splitting, hopping, and bending mechanical behaviors accompanied by a significant blue fluorescence enhancement are observed for P-BTO crystals under UV light, which is attributed to the formation of photodimer 2P-BTO. Although 2P-BTO is poorly π-conjugated because of the central cyclobutane ring, it exhibits prominent through-space conjugation and aggregation-induced emission (AIE), affording strong solid-state blue fluorescence at 415 nm with an excellent quantum yield of up to 96.2 %.

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