104115-76-6 Usage
General Description
3-Methoxynaphthalene-2-boronic acid is a chemical compound consisting of a naphthalene ring with a methoxy group and a boronic acid functional group. It is a boronic acid derivative used in organic synthesis as a building block for creating a wide range of organic compounds. This chemical has potential applications in the pharmaceutical industry, particularly in the development of pharmaceutical agents and drug candidates. It is also used in the production of agrochemicals, dyes, and materials for chemistry research. 3-Methoxynaphthalene-2-boronic acid is valuable for its reactivity in Suzuki-Miyaura cross-coupling reactions, making it an important tool for the synthesis of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 104115-76-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,1,1 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 104115-76:
(8*1)+(7*0)+(6*4)+(5*1)+(4*1)+(3*5)+(2*7)+(1*6)=76
76 % 10 = 6
So 104115-76-6 is a valid CAS Registry Number.
104115-76-6Relevant articles and documents
Thiazole-based Orange-emitting Excited-State Intramolecular Proton Transfer Chemosensors for Selective and Ratiometric Sensing of Zn2+ Ions
Kim, Sangho,Somasundaram, Sivaraman,Park, Sanghyuk
, p. 937 - 938 (2019)
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COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME
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Paragraph 0262, (2017/03/21)
When a decrease in low-grey level region (e.g., 0 to 80 grey) efficiencies of organic light emitting devices is not constant, deviation among display panels may cause color change and stain in the low luminance region. Aspects of the present disclosure ar
Unexpected results of a SNAr-reaction. A novel synthetic approach to 1-arylthio-2-naphthols
Grombein, Cornelia M.,Hu, Qingzhong,Heim, Ralf,Huch, Volker,Hartmann, Rolf W.
supporting information, p. 6615 - 6618 (2013/11/19)
1-(Phenylthio)-3-(pyridin-3-yl)-2-naphthol was obtained as an unexpected result of a nucleophilic aromatic substitution reaction of 3-(pyridine-3-yl) naphthalene-2-yl trifluoromethanesulfonate with thiophenol. This observation led to the discovery of an e