133950-77-3 Usage
Uses
Used in Biological and Biochemical Research:
5-BROMO-4-CHLORO-3-INDOXYL NONANOATE is used as a chromogenic substrate for detecting enzyme activity, specifically β-glucuronidase, allowing for the visualization and measurement of enzymatic reactions in biological and biochemical studies.
Used in Microbiology:
In the field of microbiology, 5-BROMO-4-CHLORO-3-INDOXYL NONANOATE is used as a marker for identifying the presence of specific bacteria, aiding in the diagnosis and study of microbial infections and their metabolic processes.
Used in Medical Diagnostics:
5-BROMO-4-CHLORO-3-INDOXYL NONANOATE is employed in medical diagnostics to study carbohydrate metabolism, serving as an indicator for various metabolic disorders and conditions.
Used in Pharmaceutical Research:
5-BROMO-4-CHLORO-3-INDOXYL NONANOATE is utilized as a reagent in pharmaceutical research for conducting various chemical reactions and as a tool for investigating cellular processes, contributing to the development of new drugs and therapies.
Overall, 5-BROMO-4-CHLORO-3-INDOXYL NONANOATE is a versatile chemical compound with a broad spectrum of applications in scientific research and industrial processes, playing a crucial role in enzyme detection, microbiological analysis, medical diagnostics, and pharmaceutical development.
Check Digit Verification of cas no
The CAS Registry Mumber 133950-77-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,9,5 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 133950-77:
(8*1)+(7*3)+(6*3)+(5*9)+(4*5)+(3*0)+(2*7)+(1*7)=133
133 % 10 = 3
So 133950-77-3 is a valid CAS Registry Number.
InChI:InChI=1/C17H21BrClNO2/c1-2-3-4-5-6-7-8-15(21)22-14-11-20-13-10-9-12(18)17(19)16(13)14/h9-11,20H,2-8H2,1H3
133950-77-3Relevant academic research and scientific papers
Synthesis of indigogenic substrates. Investigation of Salmonella esterase activity
Agban,Ounanian,Luu-Duc,Monget
, p. 697 - 699 (2007/10/02)
The synthesis of chromogenic compounds of indoxyl as substrates is described. A first series is obtained from unsubstituted indoxyl esters and C7-C10 fatty acids. The 5 or 6-monosubstituted bromine or chlorine derivatives of indigogenic esters and 4,5 or 5, 6-disubstituted derivatives are synthezised in the second step. Some of them are evaluated on esterase activity in Salmonella cultures. The 5-bromo-indoxyl pelargonate derivative exhibits the most interesting results.
