7471-10-5 Usage
Uses
Used in Pharmaceutical Industry:
1H-Naphth[2,3-d]imidazole-2-methanol(9CI) is used as a building block for the synthesis of various pharmaceuticals due to its unique structure and antioxidant properties, which contribute to the development of potential treatments for diseases such as cancer and neurodegenerative disorders.
Used in Agrochemical Production:
In the agrochemical industry, 1H-Naphth[2,3-d]imidazole-2-methanol(9CI) is used as an intermediate in the production of agrochemicals, playing a crucial role in the synthesis of compounds that help protect crops and enhance agricultural productivity.
Used in Dye Manufacturing:
1H-Naphth[2,3-d]imidazole-2-methanol(9CI) is also utilized as an intermediate in the manufacturing of dyes, where its chemical properties contribute to the creation of a diverse range of colorants for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 7471-10-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7471-10:
(6*7)+(5*4)+(4*7)+(3*1)+(2*1)+(1*0)=95
95 % 10 = 5
So 7471-10-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H10N2O/c15-7-12-13-10-5-8-3-1-2-4-9(8)6-11(10)14-12/h1-6,15H,7H2,(H,13,14)
7471-10-5Relevant academic research and scientific papers
BOIMPYs: Rapid Access to a Family of Red-Emissive Fluorophores and NIR Dyes
Patalag, Lukas J.,Jones, Peter G.,Werz, Daniel B.
supporting information, p. 13340 - 13344 (2016/10/30)
A fundamental, highly fluorescent, and easily accessible scaffold derived from the BODIPY core is reported. The use of benzimidazole as a bridging ligand at the meso position enables the binding of two BF2units to provide sufficient rigidity and enhanced electron-withdrawing strength. Absorption and emission events thus take place in the red (λ≈600 nm); the fluorescence quantum yields can reach unity (0.96) and show little dependence on solvent polarity. The synthetic route was shortened to two steps starting from commercially available precursors while the preparation is modular and tolerates various pyrrole and benzimidazole moieties. Fluoride replacement by propynyl groups, various halogenations, as well as Knoevenagel-type condensations were applied to extend the versatility of these new photostable fluorophores, which we termed BOIMPYs.
