151427-05-3

Basic information

• Product Name: 2-AMino-1-(4-Methoxyphenyl)ethanone hydrobroMide
• Synonyms: 2-AMino-1-(4-Methoxyphenyl)ethanone hydrobroMide
• CAS NO: 151427-05-3
• Molecular Formula: BrH*C₉H₁₁NO₂
• Molecular Weight: 246.10108
• Mol File: 151427-05-3.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-AMino-1-(4-Methoxyphenyl)ethanone hydrobroMide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMino-1-(4-Methoxyphenyl)ethanone hydrobroMide(151427-05-3)
• EPA Substance Registry System: 2-AMino-1-(4-Methoxyphenyl)ethanone hydrobroMide(151427-05-3)

Safety Data

• Hazardous Substances Data: 151427-05-3(Hazardous Substances Data)

Upstream product

• 7770-25-4 (4-methoxy-phenacyl)-hexamethylenetetraminium; bromide 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 2632-13-5 2-Bromo-4'-methoxyacetophenone 

Downstream Products

• 932389-85-0 N-(2-(4-methoxyphenyl)-2-oxoethyl)isonicotinamide 
• 151427-27-9 N-(4-methoxyphenacyl)-2,6-dimethylisonicotinamide 
• 238073-94-4 N-{2′-(4′′-methoxyphenyl)-2′-oxoethyl}-1-tosylpyrrole-2-carboxamide 
• 238073-96-6 5-(4′′-methoxyphenyl)-2-(pyrrol-2′-yl)-1,3-oxazole 
• 238073-95-5 5-(4′′-methoxyphenyl)-2-(1′-tosylpyrrol-2′-yl)-1,3-oxazole 
• 24294-82-4 2,5-bis(4-methoxyphenyl)pyrazine 
• 96753-33-2 2-(4-pyridyl)-5-(4-methoxyphenyl)-oxazole 

Relevant articles and documents

Cytotoxic 1,3-thiazole and 1,2,4-thiadiazole alkaloids from Penicillium oxalicum: Structural elucidation and total synthesis

Two new thiazole and thiadiazole alkaloids, penicilliumthiamine A and B (2 and 3), were isolated from the culture broth of Penicillium oxalicum, a fungus found in Acrida cinerea. Their structures were elucidated mainly by spectroscopic analysis, total synthesis and X-ray crystallographic analysis. Biological evaluations indicated that compound 1, 3a and 3 exhibit potent cytotoxicity against different cancer cell lines through inhibiting the phosphorylation of AKT/PKB (Ser 473), one of important cancer drugs target.

Investigations into the parallel synthesis of novel pyrrole-oxazole analogues of the insecticide pirate

Investigations into the parallel synthesis of selected analogues of a structurally unique pyrrole-oxazole analogue of the pyrrole insecticide pirate, are reported. Acylaminoketone salts were obtained from ketobromides in moderate to high yields and excell

Syntheses and Photophysical Properties of Some 5(2)-Aryl-2(5)-(4-pyridyl)oxazoles and Related Oxadiazoles and Furans

A number of 5-aryl-2-(4-pyridyl)oxazoles, a 2-aryl-5-(4-pyridyl)oxazole, the related oxadiazole and furan, several 2-(4-pyridyl)cycloalkanooxazoles, and many of their quaternary salts were prepared.No single standard synthesis was effective for preparation of more than a few of the 25 free bases described; methods often unique to a base were employed.Minor variations in structure sometimes produced large differences in absorption and emission wavelengths, as well as in the magnitude of the extinction coefficient.The salts are of interest as laser dyes, scintillation fluors, biological stains, and shifters for luminescent solar concentrators.