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17402-78-7

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17402-78-7 Usage

General Description

3-Bromo-2-nitro-benzo[b]thiophene is a chemical compound with the molecular formula C8H4BrNO2S. It is a heterocyclic organic compound that contains a benzene ring fused to a thiophene ring with a bromine atom and a nitro group attached to the thiophene ring. 3-BROMO-2-NITRO-BENZO[B]THIOPHENE is commonly used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It possesses potential biological activity and is frequently studied for its medicinal and chemical properties. Additionally, it is known for its photophysical properties and can be used in the development of materials for optoelectronic and sensor applications.

Check Digit Verification of cas no

The CAS Registry Mumber 17402-78-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,0 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17402-78:
(7*1)+(6*7)+(5*4)+(4*0)+(3*2)+(2*7)+(1*8)=97
97 % 10 = 7
So 17402-78-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H4BrNO2S/c9-7-5-3-1-2-4-6(5)13-8(7)10(11)12/h1-4H

17402-78-7SDS

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 3-bromo-2-nitro-1-benzothiophene

1.2 Other means of identification

Product number -
Other names 3-bromo-2-nitrobenzothiophene

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:17402-78-7 SDS

17402-78-7Relevant articles and documents

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van Zyl et al.

, p. 2283,2286 (1966)

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Regio- and Stereoselective Cascade of β,γ-Unsaturated Ketones by Dipeptided Phosphonium Salt Catalysis: Stereospecific Construction of Dihydrofuro-Fused [2,3-b] Skeletons

Chen, Yayun,He, Jiajia,Jiang, Chunhui,Ren, Xiaoyu,Su, Zhishan,Wang, Tianli,Xiao, Kai,Zhang, Hongkui,Zhuang, Cheng

supporting information, p. 19860 - 19870 (2021/08/06)

Chiral (dihydro)furo-fused heterocycles are significant structural motifs in numerous natural products, functional materials and pharmaceuticals. Therefore, developing efficient methods for preparing compounds with these privileged scaffolds is an important endeavor in synthetic chemistry. Herein, we develop an effective, modular method by a dipeptide-phosphonium salt-catalyzed regio- and stereoselective cascade reaction of readily available linear β,γ-unsaturated ketones with aromatic alkenes, affording a wide variety of structurally fused heterocyclic molecules in high yields with excellent stereoselectivities. Moreover, mechanistic investigations revealed that the bifunctional phosphonium salt controlled the regio- and stereoselectivities of this cascade reaction, particularly proceeding through the initial ketone α-addition followed by O-participated substitution; and the multiple hydrogen-bonding interactions between Br?nsted acid moieties of catalyst and nitro group of aromatic alkene were crucial in asymmetric induction. Given the generality, versatility, and high efficiency of this method, we anticipate that it will have broad synthetic utilities.

Substituted imidazole as a ligand containing transition metal complex and their use in OLED

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Paragraph 0106-0108, (2017/12/15)

Compounds having a metal M complexed to a ligand L containing a substituted imidazole carbene group, which is represented Formula (I), below: wherein ring B is a 5-member aromatic heterocyclic ring containing at least one heteroatom selected from the grou

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