53868-36-3 Usage
Uses
Used in Organic Chemistry:
3-(DIMETHYLAMINO)-2-(2-NITROPHENYL)ACRYLALDEHYDE is used as a reagent for the synthesis of various organic compounds, contributing to the advancement of chemical research and the creation of new chemical entities.
Used as a Fluorescent Dye:
Leveraging its fluorescent properties, 3-(DIMETHYLAMINO)-2-(2-NITROPHENYL)ACRYLALDEHYDE is utilized as a fluorescent dye molecule, which can be applied in various scientific and industrial processes that require the detection or visualization of specific substances.
Used in Material Science:
3-(DIMETHYLAMINO)-2-(2-NITROPHENYL)ACRYLALDEHYDE is considered for its potential applications in the development of new materials, where its unique properties could contribute to the creation of innovative products with enhanced characteristics.
Used in Pharmaceutical Development:
3-(DIMETHYLAMINO)-2-(2-NITROPHENYL)ACRYLALDEHYDE has been studied for its potential use in the development of pharmaceuticals, where its chemical structure and properties may offer new avenues for drug discovery and therapeutic applications.
Used in Research and Development:
3-(DIMETHYLAMINO)-2-(2-NITROPHENYL)ACRYLALDEHYDE is employed in research and development settings to explore its properties and potential applications further, including its use in creating new compounds and improving existing processes.
Check Digit Verification of cas no
The CAS Registry Mumber 53868-36-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,6 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53868-36:
(7*5)+(6*3)+(5*8)+(4*6)+(3*8)+(2*3)+(1*6)=153
153 % 10 = 3
So 53868-36-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H12N2O3/c1-12(2)7-9(8-14)10-5-3-4-6-11(10)13(15)16/h3-8H,1-2H3/b9-7+
53868-36-3Relevant academic research and scientific papers
Synthesis of tryptophans
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, (2008/06/13)
The preparation of racemic and optically pure tryptophans is described. The D-enantiomers of the 6-substituted compounds possess a potent sweetening capability. Novel intermediates are also disclosed.
