938443-32-4 Usage
Uses
Used in Organic Synthesis:
3-(Hydroxyimino)methylphenylboronic acid is used as a reagent in organic synthesis for the formation of carbon-carbon bonds. Its ability to react with a variety of organic substrates makes it a valuable tool for creating diverse chemical structures.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 3-(Hydroxyimino)methylphenylboronic acid is used as a building block for the development of new drugs. Its unique structural features allow for the creation of complex molecules with potential therapeutic applications.
Used in Agrochemical Development:
3-(Hydroxyimino)methylphenylboronic acid is also utilized in the development of agrochemicals, where it serves as a key component in the synthesis of compounds with pesticidal or herbicidal properties.
Used in Materials Science:
In the field of materials science, 3-(Hydroxyimino)methylphenylboronic acid is employed in the design and synthesis of advanced materials with specific properties, such as conductivity, catalytic activity, or self-assembly capabilities. Its versatility in forming carbon-carbon bonds and its compatibility with various substrates make it an essential component in the development of novel materials.
Check Digit Verification of cas no
The CAS Registry Mumber 938443-32-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,8,4,4 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 938443-32:
(8*9)+(7*3)+(6*8)+(5*4)+(4*4)+(3*3)+(2*3)+(1*2)=194
194 % 10 = 4
So 938443-32-4 is a valid CAS Registry Number.
938443-32-4Relevant academic research and scientific papers
A practical and cost-efficient, one-pot conversion of aldehydes into nitriles mediated by 'activated DMSO'
Augustine, John Kallikat,Bombrun, Agnes,Atta, Rajendra Nath
experimental part, p. 2223 - 2227 (2011/10/31)
Participation of activated DMSO in the one-pot transformation of aldehydes to nitriles has been described by reacting aldehydes with NHHHCl in DMSO in the absence of any added base or catalyst. The method is applicable to access a wide range of aromatic, heterocyclic, and aliphatic nitriles, in which only water is a byproduct. A straightforward and practical procedure is demonstrated on a multigram scale. Georg Thieme Verlag Stuttgart - New York.
