171881-36-0 Usage
Uses
Used in Organic Synthesis:
5-Bromo-2-(dimethylamino)benzaldehyde is used as a key intermediate in the synthesis of various organic compounds. Its reactivity, due to the presence of the bromine atom, facilitates nucleophilic substitutions, making it a valuable building block for the creation of new molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-Bromo-2-(dimethylamino)benzaldehyde is used as a precursor for the synthesis of various drug molecules. Its functional groups and reactivity enable the development of new therapeutic agents with potential applications in the treatment of various diseases.
Used in Chemical Research:
5-Bromo-2-(dimethylamino)benzaldehyde is employed as a research tool in chemical laboratories. Its unique structure and reactivity make it an interesting subject for studying reaction mechanisms, exploring new synthetic pathways, and understanding the properties of related compounds.
Used in Material Science:
5-Bromo-2-(dimethylamino)benzaldehyde can be used in the development of new materials with specific properties. Its chemical structure and reactivity may contribute to the creation of advanced materials for applications in electronics, optics, or other high-tech industries.
Used in Dye and Pigment Production:
5-BroMo-2-(diMethylaMino)benzaldehyde may also find applications in the production of dyes and pigments, where its chemical properties can be harnessed to create new colorants with improved performance characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 171881-36-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,8,8 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 171881-36:
(8*1)+(7*7)+(6*1)+(5*8)+(4*8)+(3*1)+(2*3)+(1*6)=150
150 % 10 = 0
So 171881-36-0 is a valid CAS Registry Number.
171881-36-0Relevant articles and documents
Double Capture of Difluorocarbene by 2-Aminostyrenes Enables the Construction of 3-(2,2-Difluoroethyl)-2-fluoroindoles
Sheng, Heyun,Su, Jianke,Li, Xin,Li, Xue,Song, Qiuling
supporting information, p. 7781 - 7786 (2021/10/25)
We report herein an efficient strategy to construct 3-(2,2-difluoroethyl)-2-fluoroindoles from activated o-aminostyrenes with ethyl bromodi-fluoroacetate as a difluorocarbene source. Through double capture of a difluorocarbene, two different types of fluo
BF3·OEt2-Promoted Propargyl Alcohol Rearrangement/[1,5]-Hydride Transfer/Cyclization Cascade Affording Tetrahydroquinolines
Zhao, Shuang,Wang, Xiaoyang,Wang, Pengfei,Wang, Guangwei,Zhao, Wentao,Tang, Xiangyang,Guo, Minjie
supporting information, p. 3990 - 3993 (2019/06/14)
An efficient BF3·OEt2-mediated propargyl alcohol rearrangement/[1,5]-hydride transfer/cyclization cascade for the synthesis of tetrahydroquinoline derivatives has been described. The substituents adjacent to triple bonds play an important role in the formation of ketones (via [1,3]-hydroxyl shift) or alkenyl fluorides which are products of formal trans-carbofluorination of internal alkynes. This method provides a rapid access to diverse heterocycles in moderate to excellent yields.
NOVEL CURCUMIN DERIVATIVE
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Page/Page column 111, (2009/12/07)
The present invention provides a novel compound that is structurally similar to curcumin and has a suppressive effect on Aβ aggregation, a degradative effect on Aβ aggregates, an inhibitory effect on β-secretase, and a protective effect on neurons. The novel compound is a compound represented by the following general formula (Ia) or a salt thereof: wherein R1 represents a 4-hydroxy-3-methoxyphenyl group or the like, and R2 represents a 1H-indol-6-yl group or the like.
