1368231-70-2 Usage
Uses
Used in Organic Chemistry:
4-Bromo-1H-indole-2-carbaldehyde is used as a building block for the synthesis of a range of organic compounds. Its unique molecular structure allows for the creation of various derivatives, making it a valuable component in the development of new chemical entities.
Used in Pharmaceutical Research:
4-Bromo-1H-indole-2-carbaldehyde is used as a starting material in the development of new pharmaceutical compounds. Its indole core and functional groups can be modified to create potential drug candidates, which may exhibit therapeutic properties.
Used in Materials Research:
4-Bromo-1H-indole-2-carbaldehyde is used as a component in the synthesis of new materials with potential applications in various industries. Its molecular structure can be tailored to create materials with specific properties, such as conductivity, stability, or reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 1368231-70-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,8,2,3 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1368231-70:
(9*1)+(8*3)+(7*6)+(6*8)+(5*2)+(4*3)+(3*1)+(2*7)+(1*0)=162
162 % 10 = 2
So 1368231-70-2 is a valid CAS Registry Number.
1368231-70-2Relevant academic research and scientific papers
COMPOUNDS AND USES THEREOF
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, (2021/08/06)
The present disclosure features compounds useful for the treatment of BAF complex-related disorders.
Carbene-Catalyzed Enantioselective Aromatic N-Nucleophilic Addition of Heteroarenes to Ketones
Liu, Yonggui,Luo, Guoyong,Yang, Xing,Jiang, Shichun,Xue, Wei,Chi, Yonggui Robin,Jin, Zhichao
, p. 442 - 448 (2019/11/25)
The aromatic nitrogen atoms of heteroarylaldehydes are activated by carbene catalysts to react with ketone electrophiles. Multi-functionalized cyclic N,O-acetal products are afforded in good to excellent yields and optical purities. Our reaction involves the formation of an unprecedented aza-fulvene-type acylazolium intermediate. A broad range of N-heteroaromatic aldehydes and electron-deficient ketone substrates works effectively in this transformation. Several of the chiral N,O-acetal products afforded through this protocol exhibit excellent antibacterial activities against Ralstonia solanacearum (Rs) and are valuable in the development of novel agrichemicals for plant protection.
