158920-11-7 Usage
Uses
Used in Organic Synthesis:
6,7-DIBROMO-4-METHOXY-1H-INDOLE is used as a building block in organic synthesis for the creation of various chemical compounds. Its structural features, including the bromine and methoxy groups, make it a versatile intermediate for synthesizing a wide range of molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 6,7-DIBROMO-4-METHOXY-1H-INDOLE is utilized as a key intermediate for the development of new drugs and bioactive molecules. The presence of bromine atoms and the methoxy group on the indole ring allows for the design of compounds with specific biological activities and therapeutic potentials.
Used in Pharmaceutical Development:
6,7-DIBROMO-4-METHOXY-1H-INDOLE is employed in pharmaceutical development as a precursor for the synthesis of diverse pharmaceuticals. Its unique chemical properties and structural features contribute to the discovery and optimization of new drug candidates with improved efficacy and selectivity.
Used in Research Applications:
6,7-DIBROMO-4-METHOXY-1H-INDOLE is also used in research applications to explore its chemical reactivity and potential interactions with biological targets. The presence of bromine and methoxy groups on the indole ring provides opportunities for studying its role in various chemical and biological processes.
Check Digit Verification of cas no
The CAS Registry Mumber 158920-11-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,9,2 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 158920-11:
(8*1)+(7*5)+(6*8)+(5*9)+(4*2)+(3*0)+(2*1)+(1*1)=147
147 % 10 = 7
So 158920-11-7 is a valid CAS Registry Number.
158920-11-7Relevant academic research and scientific papers
Total synthesis of (±)-dragmacidin: A cytotoxic bis(indole)alkaloid of marine origin
Jiang,Smallheer,Amaral-Ly,Wuonola
, p. 6823 - 6827 (2007/10/02)
The total synthesis of the cytotoxic marine alkaloid, (±)-dragmacidin, trans-6,7-dibromo-3-[5-(6-bromo-1H-indol-3-yl)-4-methyl-2-piperazinyl] -1H-indol-4-ol, is described. The synthesis proceeds through the condensation of (6-bromoindol-3-yl)-α-(methylami
