916818-18-3 Usage
Uses
Used in Pharmaceutical Synthesis:
1-BOC-3-CHLOROACETYLINDOLE serves as a crucial intermediate in the pharmaceutical industry, where it is utilized for the synthesis of a variety of drugs. Its unique structure allows for the development of complex molecular entities with specific therapeutic targets.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-BOC-3-CHLOROACETYLINDOLE is employed as a building block for the design and synthesis of new compounds with potential medicinal properties. Its reactivity and the presence of the BOC group make it an ideal candidate for creating molecules with controlled release mechanisms.
Used in Drug Discovery:
1-BOC-3-CHLOROACETYLINDOLE plays a significant role in drug discovery, where it is used to develop novel therapeutic agents. Its unique chemical structure contributes to the creation of diverse molecular entities that can be further optimized for improved pharmacological activities.
Used in Chemical Synthesis:
As a versatile chemical compound, 1-BOC-3-CHLOROACETYLINDOLE is used in chemical synthesis for creating a wide range of organic compounds. Its BOC protective group allows for selective reactions, making it a valuable asset in the synthesis of complex organic molecules.
Used in Biological Research:
In biological research, 1-BOC-3-CHLOROACETYLINDOLE is utilized for studying the interactions between various molecular entities and biological systems. Its controlled release properties make it an attractive tool for investigating the effects of indole compounds on biological processes.
Check Digit Verification of cas no
The CAS Registry Mumber 916818-18-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,8,1 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 916818-18:
(8*9)+(7*1)+(6*6)+(5*8)+(4*1)+(3*8)+(2*1)+(1*8)=193
193 % 10 = 3
So 916818-18-3 is a valid CAS Registry Number.
916818-18-3Relevant academic research and scientific papers
Johnson, Ann-Louise,Bergman, Jan
, p. 10815 - 10820 (2006)
The exocyclic analogue of the indole alkaloid isolated from the marine sponge Halichondria melanodocia has been prepared via olefination of a phosphonoester derived from 3-(2-bromoacyl)indole. The formation of an unexpected indolylazepine is also discusse
