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1228552-87-1

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1228552-87-1 Usage

General Description

1-(7-bromoquinolin-3-yl)ethanone is a chemical compound with the molecular formula C11H8BrNO. It belongs to the group of ketones and features a 7-bromoquinoline ring attached to an ethanone group. 1-(7-bromoquinolin-3-yl)ethanone is commonly used in organic synthesis and pharmaceutical research, where it serves as a building block for the production of various pharmacologically active substances. Its unique structure and reactivity make it a valuable intermediate in the development of medicinal compounds and agrochemicals. Additionally, it has also been studied for its potential antimalarial and antimicrobial properties. Overall, 1-(7-bromoquinolin-3-yl)ethanone is a versatile and important compound with potential applications in drug development and other areas of chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 1228552-87-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,8,5,5 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1228552-87:
(9*1)+(8*2)+(7*2)+(6*8)+(5*5)+(4*5)+(3*2)+(2*8)+(1*7)=161
161 % 10 = 1
So 1228552-87-1 is a valid CAS Registry Number.

1228552-87-1Downstream Products

1228552-87-1Relevant articles and documents

Biocatalytic synthesis of quinoline derivatives via α-amylase catalysed one-pot domino aza-Michael/Aldol/aromatization reactions

Dutt, Sunil,Tyagi, Vikas

supporting information, (2021/12/01)

Quinoline moiety is a part of various drug molecules and natural products. Previously, a number of catalysts have been made available to synthesize substituted quinolines. Herein, we are reporting α-amylase catalysed synthesis of substituted quinolines via one-pot domino aza-Michael/Aldol/aromatization reactions. Moreover, the α-amylase enzyme from Aspergillus oryzae was found to catalyse the cascade reaction of various 2-aminobenzaldehydes with α, β-unsaturated carbonyls in high catalytic efficiency (56–86% yield).

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