111005-19-7 Usage
Uses
Used in Organic Synthesis:
3,5-Dimethanolpyridine is used as a building block in organic synthesis for the preparation of a wide range of pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structural features and reactivity contribute to the development of novel compounds with potential applications in various industries.
Used in Coordination Chemistry:
In the field of coordination chemistry, 3,5-Dimethanolpyridine serves as a ligand for the synthesis of metal-organic complexes. Its ability to form stable complexes with metal ions enhances the properties of these complexes, making them suitable for various applications in catalysis, materials science, and other areas.
Used in Chemical Industry:
3,5-Dimethanolpyridine has a wide range of applications in the chemical industry due to its versatility and reactivity. It is utilized in the production of various chemical intermediates and specialty chemicals, contributing to the development of innovative products and processes.
Used in Research Laboratories:
In research settings, 3,5-Dimethanolpyridine is employed as a valuable compound for exploring new synthetic routes, studying reaction mechanisms, and developing novel applications. Its unique properties make it an essential tool for researchers working in the fields of organic chemistry, medicinal chemistry, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 111005-19-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,0,0 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 111005-19:
(8*1)+(7*1)+(6*1)+(5*0)+(4*0)+(3*5)+(2*1)+(1*9)=47
47 % 10 = 7
So 111005-19-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO2/c9-4-6-1-7(5-10)3-8-2-6/h1-3,9-10H,4-5H2
111005-19-7Relevant articles and documents
Dipolar Cycloaddition Reactions of Diazoazoles with Electron-Rich and with Strained Unsaturated Compounds
Magee, W. L.,Rao, C. B.,Glinka, J.,Hui, H.,Amick, T. J.,et al.
, p. 5538 - 5548 (2007/10/02)
Regiospecific net 1,7-cycloaddition reactions of electron-rich or strained olefins and electron-donor acetylenes occur readily (-70 to -10 degC) with diazoazoles having nitrogen in the 2-positions of their azole rings.Diazoazoles such as 5-tert-butyl-3-diazo-3H-pyrazole (20), 3-diazo-5-phenyl-3H-pyrazole (24), 2-diazo-2H-imidazole (28), 4,5-dicyano-2-diazo-2H-imidazole (12), 4-diazo-4H-imidazole (63), 4-diazo-5-phenyl-4H-1,2,3-triazole (70), 5-cyano-4-diazo-4H-1,2,3-triazole (74), 3-diazo-3H-1,2,4-triazole (76), and 3-diazo-5-phenyl-3H-1,2,4-triazole (79) thus usually add effectively to unsaturated reactans such as enamines, 1-alkoxyalkenes, ketene acetals, aryl isocyanates, norbornene, and norbornadiene to give new 1,7-cycloadducts.These cyclization reactions may be followed by tautomerization processes leading to new stabilized fused heterocycles or by elimination to novel highly delocalized heteroaromatic derivatives. 4,5-Dicyano-2-diazo-2H-imidazole (12) undergoes various accelerated cycloadditions to unsaturates and adds to norbornene and norbornadiene by exclusive exo dipolar processes.Addition of activated acetylenes to representative α-diazoazoles also results in regiospecific 1,7-cyclization to give stabilized fused azolo heterocycles.
