1093452-52-8 Usage
Uses
Used in Organic Synthesis:
Indole-3-carboxaldehyde-13C is used as a labeled compound for organic synthesis. The incorporation of carbon-13 into the molecule allows for the tracking of its behavior and interactions within chemical reactions, which can be beneficial for understanding reaction mechanisms and optimizing synthetic routes.
Used in Pharmaceutical Research:
In the pharmaceutical industry, Indole-3-carboxaldehyde-13C can be used as a labeled reference compound for the development and testing of new drugs. The carbon-13 label can help researchers identify and track the compound within biological systems, aiding in the study of drug metabolism, pharmacokinetics, and pharmacodynamics.
Used in Environmental Science:
Indole-3-carboxaldehyde-13C can also be employed in environmental science for tracing the fate and transport of similar compounds in ecosystems. The carbon-13 label can provide insights into the environmental impact and degradation pathways of related chemicals, contributing to the development of more sustainable and eco-friendly products.
Used in Analytical Chemistry:
In analytical chemistry, Indole-3-carboxaldehyde-13C can serve as an internal standard or a reference material for the quantification and identification of related compounds using techniques such as mass spectrometry. The carbon-13 label can improve the accuracy and precision of analytical measurements, ensuring reliable results in various research and quality control applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1093452-52-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,3,4,5 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1093452-52:
(9*1)+(8*0)+(7*9)+(6*3)+(5*4)+(4*5)+(3*2)+(2*5)+(1*2)=148
148 % 10 = 8
So 1093452-52-8 is a valid CAS Registry Number.
1093452-52-8Relevant articles and documents
Mild and selective Ru-catalyzed formylation and Fe-catalyzed acylation of free (N-H) indoles using anilines as the carbonyl source
Wu, Wenliang,Su, Weiping
supporting information; experimental part, p. 11924 - 11927 (2011/09/19)
C3-selective formylation and acylation of free (N-H) indoles under mild conditions can be achieved by using Ru- and Fe-catalyzed oxidative coupling of free (N-H) indoles with anilines, respectively. Both processes are operationally simple, compatible with a variety of functional groups and generally provide the desired products in good yields. 13C-labeling experiments unambiguously established that the carbonylic carbon in the formylation products originated from methyl group of N-methyl aniline.
