13052-19-2 Usage
Uses
Used in Pharmaceutical Industry:
N-(hydroxymethyl)formamide is used as a solvent for the dissolution and processing of various pharmaceutical compounds. Its high solubility and compatibility with a range of substances make it a valuable component in the development and manufacturing of medications.
Used in Chemical Industry:
In the chemical industry, N-(hydroxymethyl)formamide serves as a versatile solvent for a variety of chemical reactions and processes. Its ability to dissolve a wide array of compounds facilitates the synthesis and production of numerous chemical products.
Used in Chemical Synthesis:
N-(hydroxymethyl)formamide is used as a reagent and intermediate in the synthesis of various chemicals and pharmaceuticals. Its unique chemical properties allow it to participate in a range of reactions, contributing to the formation of desired products.
Used in Research and Development:
Due to its solvent properties and reactivity, N-(hydroxymethyl)formamide is employed in research and development settings to explore new chemical reactions, synthesize novel compounds, and study the properties of existing substances.
Check Digit Verification of cas no
The CAS Registry Mumber 13052-19-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,5 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13052-19:
(7*1)+(6*3)+(5*0)+(4*5)+(3*2)+(2*1)+(1*9)=62
62 % 10 = 2
So 13052-19-2 is a valid CAS Registry Number.
InChI:InChI=1/C2H5NO2/c4-1-3-2-5/h1,5H,2H2,(H,3,4)
13052-19-2Relevant academic research and scientific papers
Hartung, Rainer,Golz, Gregor,Schlaf, Susanne,Silvennoinen, Gudrun,Polborn, Kurt,Mayer, Peter,Pfaendler, Hans Rudolf
, p. 495 - 501 (2009)
New formaldehyde derivatives were prepared in good yields by a short and versatile route. Several crystal structures of corresponding thioacetic acid esters and thiols were determined. The thioacetates were cleaved under acidic or basic conditions affording the thiols in high yield, thus introducing the new substance classes of N-mercaptomethyl-alkylcarboxamides, N-mercapto- methylsulfonamides, and alkoxymethanethiols. Georg Thieme Verlag Stuttgart New York.
