81387-89-5 Usage
Uses
Used in Pharmaceutical Industry:
3,5-Dibromoindole is used as a building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 3,5-Dibromoindole serves as a key component in the creation of agrochemicals, potentially enhancing crop protection and yield.
Used in Organic Materials Synthesis:
3,5-Dibromoindole is utilized as a building block in the synthesis of organic materials, which can be applied in various industries for different purposes, such as in the production of dyes, pigments, or other specialty chemicals.
Used in Antibacterial Applications:
3,5-Dibromoindole is being studied for its potential as an anti-bacterial agent, which could be used to combat bacterial infections and contribute to the development of new antibiotics.
Used in Anticancer Research:
As a compound with potential biological activities, 3,5-Dibromoindole is under investigation for its possible role as an anti-cancer agent, with the aim of identifying its effects on cancer cells and its potential use in cancer treatment.
Check Digit Verification of cas no
The CAS Registry Mumber 81387-89-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,3,8 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81387-89:
(7*8)+(6*1)+(5*3)+(4*8)+(3*7)+(2*8)+(1*9)=155
155 % 10 = 5
So 81387-89-5 is a valid CAS Registry Number.
81387-89-5Relevant academic research and scientific papers
Synthesis of bromoindole alkaloids from Laurencia brongniartii
Suarez-Castillo, Oscar R.,Beiza-Granados, Lidia,Melendez-Rodriguez, Myriam,Alvarez-Hernandez, Alejandro,Morales-Rios, Martha S.,Joseph-Nathan, Pedro
, p. 1596 - 1600 (2008/09/18)
A regioselective synthesis of N-carbomethoxy-2,3,5-tribromoindole (6) via a sequential one-pot bromination-aromatization-bromination of N-carbomethoxyindoline (2) is described. The process for the transformation of 2 into 6 permitted the isolation of stable reaction intermediates N-carbomethoxy-5-bromoindoline (3), N-carbomethoxy-5-bromoindole (4), and N-carbomethoxy-3,5-dibromoindole (5). Compound 6 was used to complete the total synthesis of the natural products 1b and 1c. In addition, bromination of N-carbomethoxyindole (11) afforded N-carbomethoxy-2,3,6-tribromoindole (13), from which the natural product 1a was synthesized.
