55368-83-7

Basic information

• Product Name: 4-Bromobenzimidic acid ethyl ester hydrochloride
• Synonyms: 4-Bromobenzimidic acid ethyl ester hydrochloride;Ethyl 4-bromobenzimidate hydrochloride;Ethyl 4-bromobenzenecarboximidate hydrochloride;ethyl 4-bromobenzene-1-carboximidate hydrochloride
• CAS NO: 55368-83-7
• Molecular Formula: C9H11BrClNO
• Molecular Weight: 264.54674
• Mol File: 55368-83-7.mol
• Article Data: 20

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-Bromobenzimidic acid ethyl ester hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Bromobenzimidic acid ethyl ester hydrochloride(55368-83-7)
• EPA Substance Registry System: 4-Bromobenzimidic acid ethyl ester hydrochloride(55368-83-7)

Safety Data

• Hazardous Substances Data: 55368-83-7(Hazardous Substances Data)

Upstream product

• 623-00-7 4-bromobenzenecarbonitrile 
• 75-36-5 acetyl chloride 
• 67-56-1 methanol 
• 64-17-5 ethanol 

Downstream Products

• 1184174-37-5 1-[3-(4-bromo-phenyl)-[1,2,4]triazol-1-yl]-2-methyl-propan-2-ol 
• 1184174-47-7 2-(3-(4-bromophenyl)-1H-1,2,4-triazol-1-yl)ethanol 
• 1184174-48-8 2-(3-(4-bromophenyl)-1H-1,2,4-triazol-1-yl)ethyl formate 
• 1184174-17-1 3-(4-bromo-phenyl)-1,5-dimethyl-1H-[1,2,4]triazole 
• 1184174-30-8 3-(4-bromo-phenyl)-1-isopropyl-1H-[1,2,4]triazole 
• 83253-23-0 4-Amino-2-(4-Bromophenyl)-1,3,5-triazine 
• 1184174-04-6 3-(4-bromophenyl)-1-methyl-1H-[1,2,4]triazole 

Relevant articles and documents

DNA-Encoded Libraries: Hydrazide as a Pluripotent Precursor for On-DNA Synthesis of Various Azole Derivatives

DNA-encoded combinatorial chemical library (DEL) technology, an approach that combines the power of genetics and chemistry, has emerged as an invaluable tool in drug discovery. Skeletal diversity plays a fundamental importance in DEL applications, and relies heavily on novel DNA-compatible chemical reactions. We report herein a phylogenic chemical transformation strategy using DNA-conjugated benzoyl hydrazine as a common versatile precursor in azole chemical expansion of DELs. DNA-compatible reactions deriving from the common benzoyl hydrazine precursor showed excellent functional group tolerance with exceptional efficiency in the synthesis of various azoles, including oxadiazoles, thiadiazoles, and triazoles, under mild reaction conditions. The phylogenic chemical transformation strategy provides DELs a facile way to expand into various unique chemical spaces with privileged scaffolds and pharmacophores.

Microwave-assisted synthesis of new 2-aryl and 2-alkylimidazolones and evaluation of their in vitro anticancer activity and their in vivo toxicity on zebrafish embryos

Herein we describe the synthesis of five new 2-aryl and 2-alkylimidazolone derivatives via an effective one-pot synthetic strategy assisted by microwave irradiations which allowed us to access the desired product in a reduced time reaction compared to the

Fluorescent organic light emitting elements having high efficiency

An organic light-emitting element which emits delayed fluorescence comprising specifically substituted 1,2,4-triazole derivatives, 1,2,4-oxadiazole derivatives or 1,2,4-thiadiazole derivatives in the light-emitting layer, a light-emitting layer comprising