Welcome to LookChem.com Sign In|Join Free
  • or
3-BROMO-2-NITROTHIOPHENE, with the molecular formula C4H2BrNO2S, is a yellow solid chemical compound that serves as a crucial intermediate in the synthesis of pharmaceuticals and agrochemicals. Known for its reactivity, it is instrumental in the creation of heterocyclic compounds, particularly thieno[2,3-b]pyridines, which exhibit potential as antimicrobial, antiviral, and anticancer agents. Furthermore, 3-BROMO-2-NITROTHIOPHENE finds application in the preparation of dyes and pigments. Due to its hazardous nature, it requires careful handling to prevent irritation to the eyes, skin, and respiratory system.

24430-27-1

Post Buying Request

24430-27-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

24430-27-1 Usage

Uses

Used in Pharmaceutical Industry:
3-BROMO-2-NITROTHIOPHENE is used as a chemical intermediate for the synthesis of various pharmaceuticals, specifically targeting the development of heterocyclic compounds with potential applications as antimicrobial, antiviral, and anticancer agents. Its reactivity in chemical reactions facilitates the creation of these therapeutically valuable compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 3-BROMO-2-NITROTHIOPHENE is utilized as an intermediate in the synthesis of agrochemicals, contributing to the development of products that protect crops and enhance agricultural productivity.
Used in Dye and Pigment Industry:
3-BROMO-2-NITROTHIOPHENE is employed as a key component in the preparation of dyes and pigments, providing a wide range of color options for various applications, including textiles, plastics, and printing inks.
Safety Precautions:
Given its classification as a hazardous substance, 3-BROMO-2-NITROTHIOPHENE requires careful handling to minimize exposure and prevent potential irritation to the eyes, skin, and respiratory system. Proper safety measures, including the use of personal protective equipment and adherence to safety protocols, are essential when working with 3-BROMO-2-NITROTHIOPHENE.

Check Digit Verification of cas no

The CAS Registry Mumber 24430-27-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,3 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 24430-27:
(7*2)+(6*4)+(5*4)+(4*3)+(3*0)+(2*2)+(1*7)=81
81 % 10 = 1
So 24430-27-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H2BrNO2S/c5-3-1-2-9-4(3)6(7)8/h1-2H

24430-27-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-BROMO-2-NITROTHIOPHENE

1.2 Other means of identification

Product number -
Other names bromo-3 nitro-2 thiophene

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:24430-27-1 SDS

24430-27-1Upstream product

24430-27-1Relevant academic research and scientific papers

AROMATIC 2-NITROSULFONYL FLUORIDE ANTIBIOTICS AND METHODS OF USE THEREOF

-

Paragraph 0008, (2019/01/16)

Aspects of the present disclosure include antibacterial aromatic sulfonyl fluoride agents. The subject aromatic sulfonyl fluoride agents have a pharmacophore that can provide for potent antibacterial activity. The subject agents are compounds including an

Thieno[3,2-b]pyrrole-5-carboxamides as New Reversible Inhibitors of Histone Lysine Demethylase KDM1A/LSD1. Part 1: High-Throughput Screening and Preliminary Exploration

Sartori, Luca,Mercurio, Ciro,Amigoni, Federica,Cappa, Anna,Fagá, Giovanni,Fattori, Raimondo,Legnaghi, Elena,Ciossani, Giuseppe,Mattevi, Andrea,Meroni, Giuseppe,Moretti, Loris,Cecatiello, Valentina,Pasqualato, Sebastiano,Romussi, Alessia,Thaler, Florian,Trifiró, Paolo,Villa, Manuela,Vultaggio, Stefania,Botrugno, Oronza A.,Dessanti, Paola,Minucci, Saverio,Zagarrí, Elisa,Carettoni, Daniele,Iuzzolino, Lucia,Varasi, Mario,Vianello, Paola

supporting information, p. 1673 - 1692 (2017/03/17)

Lysine specific demethylase 1 KDM1A (LSD1) regulates histone methylation and it is increasingly recognized as a potential therapeutic target in oncology. We report on a high-throughput screening campaign performed on KDM1A/CoREST, using a time-resolved fluorescence resonance energy transfer (TR-FRET) technology, to identify reversible inhibitors. The screening led to 115 hits for which we determined biochemical IC50, thus identifying four chemical series. After data analysis, we have prioritized the chemical series of N-phenyl-4H-thieno[3, 2-b]pyrrole-5-carboxamide for which we obtained X-ray structures of the most potent hit (compound 19, IC50 = 2.9 μM) in complex with the enzyme. Initial expansion of this chemical class, both modifying core structure and decorating benzamide moiety, was directed toward the definition of the moieties responsible for the interaction with the enzyme. Preliminary optimization led to compound 90, which inhibited the enzyme with a submicromolar IC50 (0.162 μM), capable of inhibiting the target in cells.

Heterocyclic-ring condensed benzothiazine compound

-

, (2008/06/13)

The invention provides a novel heterocyclic ring condensed benzothiazine compound which is effective for prevention or remedy of disease, in which histamine, leukotriene and the like participate. The heterocyclic ring condensed benzothiazine compound of the present invention or a pharmacologically acceptable salt thereof is effective for prevention or remedy of disease, in which a chemical mediator, such as histamine, leukotriene and the like, participate, for example, asthma, allergic coryza, atopic dermatitis, hives, hay fever, gastrointestinal allergy, food allergy and the like. Further, the heterocyclic ring condensed benzothiazine compound of the present invention, its pharmacologically acceptable salt or hydrates thereof is represented by the following formula: In the formula, the ring Het represents an unsaturated heterocyclic ring; R1and R2are the same as or different from each other, and each represents halogen atom, a lower alkyl group that may be substituted with a halogen atom, a lower alkoxy group that may be substituted with a halogen atom, a lower alkyl lower alkoxy group, cyano group; D represents a lower alkylene group and the like that may have a substituent; Q represents, for example, the formula —NR20R2(in the formula, R20and R21are the same as or different from each other, and each represents hydrogen atom, a lower alkyl group that may be substituted with a halogen atom, an aryl group that may have a substituent, an arylalkyl group that may have a substituent, a heteroaryl group that may have a substituent or a heteroarylalkyl group that may have a substituent, or R20and R21may form a 3- to 8-membered ring along with the nitrogen atom to which they are bound); and x represents an integer of from 1 to 2.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 24430-27-1