ChemicalBook > Product Catalog >Pharmaceutical intermediates >Heterocyclic compound >Thiophene compounds >4-BROMO-5-NITROTHIOPHENE-2-CARBOXALDEHYDE

4-BROMO-5-NITROTHIOPHENE-2-CARBOXALDEHYDE

4-BROMO-5-NITROTHIOPHENE-2-CARBOXALDEHYDE Suppliers list
Company Name: Shanghai Longsheng chemical Co.,Ltd.  
Tel: 58099637 13585536065
Email: sales@shlschem.com
Company Name: Chengdu Forest Science and Technology Development Co., Ltd.  
Tel: 18030648795 18030648795
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Company Name: Chengdu HuaXia Chemical Reagent Co. Ltd  
Tel: 400-1166-196 13458535857
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Company Name: Shanghai Yongye Biotechnology Co., Ltd.  
Tel: 86-021-61559134 15921386130
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Company Name: Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.  
Tel: 025-66028182 17714375163
Email: yftan@aikonchem.com

4-BROMO-5-NITROTHIOPHENE-2-CARBOXALDEHYDE manufacturers

4-BROMO-5-NITROTHIOPHENE-2-CARBOXALDEHYDE Basic information
Product Name:4-BROMO-5-NITROTHIOPHENE-2-CARBOXALDEHYDE
Synonyms:4-BROMO-5-NITRO-2-THIOPHENECARBOXALDEHYDE;4-BROMO-5-NITROTHIOPHENE-2-CARBOXALDEHYDE;4-BroMo-5-nitrothiophene-2-carbaldehyde;2-Thiophenecarboxaldehyde, 4-bromo-5-nitro-;4-BROMO-5-NITROTHIOPHENE-2-CARBOXALDEHYDE ISO 9001:2015 REACH
CAS:41498-07-1
MF:C5H2BrNO3S
MW:236.04
EINECS:200-589-5
Product Categories:Thiophenes
Mol File:41498-07-1.mol
4-BROMO-5-NITROTHIOPHENE-2-CARBOXALDEHYDE Structure
4-BROMO-5-NITROTHIOPHENE-2-CARBOXALDEHYDE Chemical Properties
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
AppearanceLight yellow to yellow Solid
Safety Information
MSDS Information
4-BROMO-5-NITROTHIOPHENE-2-CARBOXALDEHYDE Usage And Synthesis
Synthesis
4-Bromothiophene-2-carboxaldehyde

18791-75-8

4-BROMO-5-NITROTHIOPHENE-2-CARBOXALDEHYDE

41498-07-1

General procedure for the synthesis of 4-bromo-5-nitro-2-thiophenecarboxaldehyde from 4-bromo-2-thiophenecarboxaldehyde: A nitration reagent was prepared by dissolving potassium nitrate (110 g, 1.09 mol) in concentrated sulfuric acid (550 mL). The above nitration reagent was slowly added to a mixed solution of anhydrous dichloromethane (5 mL) and concentrated sulfuric acid (1.1 L) containing 4-bromo-2-thiophenecarboxaldehyde (207.6 g, 1.08 mol) at 0 °C, and the addition process was controlled to be completed within 45 min. The reaction mixture was continued to be stirred at 0 °C for 2 h, followed by raising to room temperature and stirring overnight. Upon completion of the reaction, the mixture was slowly poured into ice water, the precipitate was collected by filtration and washed sequentially with water and hexane. The resulting yellow solid was dried overnight to afford the target product 4-bromo-5-nitro-2-thiophenecarboxaldehyde (251.4 g, 98.6% yield). The structure of the product was confirmed by 1H-NMR (DMSO-d6): δ 9.90 (s, 1H, aldehydic hydrogen), 8.56 (s, 1H, thiophene cyclohexane).

References[1] Patent: US2004/9995, 2004, A1
[2] Patent: WO2003/99805, 2003, A1. Location in patent: Page 384
[3] Patent: WO2006/101860, 2006, A1. Location in patent: Page/Page column 91-92
[4] Patent: US2013/324501, 2013, A1. Location in patent: Paragraph 0327; 0328
[5] Patent: WO2013/182451, 2013, A1. Location in patent: Page/Page column 85
4-BROMO-5-NITROTHIOPHENE-2-CARBOXALDEHYDE Preparation Products And Raw materials
Raw materials4-Bromothiophene-2-carboxaldehyde-->Sulfuric acid-->Potassium nitrate-->Dichloromethane
Tag:4-BROMO-5-NITROTHIOPHENE-2-CARBOXALDEHYDE(41498-07-1) Related Product Information
Bispyrithione 7-FLUORO INDAZOLE Phenylpentane DBDCB 2-Methylbutyraldehyde 4,5,6-Trichloropyrimidine Dimethyl 4-nitrophthalate 2,4,6-Trifluorobenzoic acid 2,3,4,5-Tetrafluorobenzoic acid BOC-GAMMA-ABU-OH 5-Bromo-2-(methylthio)pyrimidine-4-carboxylic acid 4-Nitrophenylboronic acid 2-Fluoro-4-nitrobenzaldehyde 5-Bromo-6-methoxynicotinic acid methyl ester CALCIUM ALUMINATE 5-NITROTHIOPHENE-2-CARBOXALDEHYDE