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2-(3,4-dimethoxyphenyl)quinoline-4-carbonyl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1160264-86-7

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1160264-86-7 Usage

Chemical class

Quinoline derivatives

Structure

2-(3,4-dimethoxyphenyl)quinoline-4-carbonyl chloride is a carbonyl chloride derivative of 2-(3,4-dimethoxyphenyl)quinoline-4-carboxylic acid.

Usage

Potential applications in organic synthesis, medicinal chemistry, and pharmaceutical research.

Property exploration

Specific properties and potential applications would need to be further explored through research and experimentation.

Check Digit Verification of cas no

The CAS Registry Mumber 1160264-86-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,0,2,6 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1160264-86:
(9*1)+(8*1)+(7*6)+(6*0)+(5*2)+(4*6)+(3*4)+(2*8)+(1*6)=127
127 % 10 = 7
So 1160264-86-7 is a valid CAS Registry Number.

1160264-86-7Downstream Products

1160264-86-7Relevant academic research and scientific papers

Quinoline-4-carboxamide skeleton derivative and application thereof

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Paragraph 0115-0118, (2021/06/09)

The invention discloses a quinoline-4-formamide skeleton derivative and application thereof, belonging to the field of chemical medicines. The invention provides a compound as shown in a formula I or pharmaceutically acceptable salt thereof. The invention

Discovery of Potent Small-Molecule SIRT6 Activators: Structure-Activity Relationship and Anti-Pancreatic Ductal Adenocarcinoma Activity

Chen, Xiuli,Sun, Weining,Huang, Shenzhen,Zhang, Hailin,Lin, Guifeng,Li, Hui,Qiao, Jingxin,Li, Linli,Yang, Shengyong

, p. 10474 - 10495 (2020/11/02)

SIRT6 activation is thought to be a promising target for the treatment of many diseases, particularly cancer. Herein, we report the discovery of a series of new small-molecule SIRT6 activators. Structure-activity relationship analyses led to the identific

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