6344-41-8 Usage
Description
[benzyl(nitroso)amino]acetic acid, with the chemical formula C9H10N2O3, is a derivative of aminoacetic acid. It features a benzene group connected to a nitroso functional group and an amine group. [benzyl(nitroso)amino]acetic acid holds potential in various fields due to its unique structure and properties.
Uses
Used in Chemical Synthesis:
[benzyl(nitroso)amino]acetic acid is used as a reagent in chemical reactions for its distinctive structure and properties, making it a valuable component in the synthesis of various compounds.
Used in Organic Chemistry:
Its unique structure also makes [benzyl(nitroso)amino]acetic acid a potentially useful compound in the field of organic chemistry, where it can contribute to the development of novel organic compounds and reactions.
Used in Pharmaceutical Industry:
[benzyl(nitroso)amino]acetic acid is used as a precursor in the development of new drugs or medical treatments within the pharmaceutical industry. Its potential in this application is still under investigation, and further research is required to fully understand and optimize its uses.
Used in Research and Development:
[benzyl(nitroso)amino]acetic acid is utilized in research and development for its potential applications in various industries. Its unique properties and structure make it an interesting compound for scientists to study and explore its possible uses and benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 6344-41-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6344-41:
(6*6)+(5*3)+(4*4)+(3*4)+(2*4)+(1*1)=88
88 % 10 = 8
So 6344-41-8 is a valid CAS Registry Number.
6344-41-8Relevant articles and documents
SUBSTITUTED CYCLOALKYLS AS MODULATORS OF THE INTEGRATED STRESS PATHWAY
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Page/Page column 372, (2020/11/12)
Provided herein are compounds, compositions, and methods useful for modulating the integrated stress response (ISR) and for treating related diseases, disorders and conditions.
Synthesis of 2 H-indazoles by the [3 + 2] dipolar cycloaddition of sydnones with arynes
Fang, Yuesi,Wu, Chunrui,Larock, Richard C.,Shi, Feng
experimental part, p. 8840 - 8851 (2012/01/02)
A rapid and efficient synthesis of 2H-indazoles has been developed using a [3 + 2] dipolar cycloaddition of sydnones and arynes. A series of 2H-indazoles have been prepared in good to excellent yields using this protocol, and subsequent Pd-catalyzed coupl
Reaction of Sydnones with Oxygen
Nakajima, Masayuki,Anselme, Jean-Pierre
, p. 1444 - 1448 (2007/10/02)
The reaction of 3-benzyl- and 3-(p-chlorobenzyl)-4-phenylsydnones (1a and 1b) and of 3-benzylsydnone (1c) with oxygen at room temperature in the dark is described.Possible rationalizations for the formation of the products obtained are suggested.
