7471-10-5 Usage
General Description
1H-Naphth[2,3-d]imidazole-2-methanol(9CI) is a chemical compound with a naphthalene ring fused to an imidazole ring, and a methanol group attached to the imidazole ring. It is commonly used as a building block in the synthesis of various pharmaceuticals and organic compounds. This chemical is known for its antioxidant properties and has been studied for its potential applications in the treatment of a variety of diseases, including cancer and neurodegenerative disorders. It is also used as an intermediate in the production of agrochemicals and dyes. 1H-Naphth[2,3-d]imidazole-2-methanol(9CI) is available in solid form and is typically handled and stored under controlled conditions due to its potential reactivity and toxicity.
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 articles and documents
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.
