6344-41-8

Usage

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.

Upstream product

• 17136-36-6 N-benzylglycine 
• 7689-50-1 N-benzyl glycine hydrochloride 
• 100-46-9 benzylamine 
• 3287-99-8 benzylamine hydrochloride 
• 63086-36-2 2-(benzylamino)acetonitrile hydrochloride 

Downstream Products

• 42151-75-7 α-(1-Benzyl-hydrazino)-essigsaeure 
• 28667-51-8 10-benzyl-9,10-diazatetracyclo<6.3.0.0.^4,110.^5,9>undecane 

Relevant academic research and scientific papers

SUBSTITUTED CYCLOALKYLS AS MODULATORS OF THE INTEGRATED STRESS PATHWAY

Provided herein are compounds, compositions, and methods useful for modulating the integrated stress response (ISR) and for treating related diseases, disorders and conditions.

Sydnone Cycloaddition Route to Pyrazole-Based Analogs of Combretastatin A4

The combretastatins are an important class of tubulin-binding agents. Of this family, a number of compounds are potent tumor vascular disrupting agents (VDAs) and have shown promise in the clinic for cancer therapy. We have developed a modular synthetic r

Synthesis of 2 H-indazoles by the [3 + 2] dipolar cycloaddition of sydnones with arynes

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

Synthesis and reactions of 9,10-diazatetracyclo-[6.3.0.0.4,110.5.9]undecanes

The tandem 1,3-dipolar cycloaddition between sydnones and 1,5-cyclooctadiene provides 9,10-diazatetracyclo[6.3.0.0.4,110.5,9]undecanes (the Weintraub reaction) in modest to good yields.

Reaction of Sydnones with Oxygen

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.