23145-18-8 Usage
Uses
Used in Organic Synthesis:
5-nitro-1-benzofuran-2-carbaldehyde is used as a key intermediate in the synthesis of various organic compounds, primarily for the preparation of pharmaceuticals and agrochemicals. Its structural features facilitate the development of a wide range of molecules with potential applications in these fields.
Used in Fluorescence Spectroscopy:
Leveraging its fluorescent properties, 5-nitro-1-benzofuran-2-carbaldehyde is employed as a component in the creation of fluorescent probes and sensors. These tools are designed to detect specific molecules and ions within biological and environmental samples, contributing to advancements in analytical chemistry and related disciplines.
Used in Chemical Research:
5-nitro-1-benzofuran-2-carbaldehyde's versatile reactivity and fluorescent characteristics render it an indispensable tool in chemical research. It aids in the exploration of new chemical reactions and the development of innovative materials and compounds.
Used in Industrial Applications:
Beyond research, 5-nitro-1-benzofuran-2-carbaldehyde finds utility in various industrial applications where its unique properties can be harnessed for the production of specialty chemicals, materials, and other products that require specific optical or chemical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 23145-18-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,1,4 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 23145-18:
(7*2)+(6*3)+(5*1)+(4*4)+(3*5)+(2*1)+(1*8)=78
78 % 10 = 8
So 23145-18-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H5NO4/c11-5-8-4-6-3-7(10(12)13)1-2-9(6)14-8/h1-5H
23145-18-8Relevant academic research and scientific papers
Benzoxazepinones and their use as squalene synthase inhibitors
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, (2008/06/13)
There is disclosed a compound represented by the formula [I]: wherein R1 is optionally substituted 1-carboxyethyl group, optionally substituted alkyl-sulfonyl group, optionally substituted (carboxy-cycloalkyl)-alkyl group, -X1-X2-Ar-X3-X4-COOH (wherein X1 and X4 are a bond or alkylene group, X2 and X3 are a bond, -O-, -S-, Ar is divalent aromatic group etc.), R2 is alkyl group optionally substituted with alkanoyloxy group and/or hydroxy group, R3 is alkyl group, and W is halogen atom, etc., or a salt thereof. The compound has the cholesterol lowering activity and the triglyceride lowering activity and is useful for preventing and/or treating hyperlipidemia.
