2512-23-4 Usage
Uses
Used in Organic Synthesis:
Methanesulfonamide, N-(1,1-dimethylethyl)is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the formation of desired products in the synthesis of complex organic molecules.
Used in Pharmaceutical Manufacturing:
In the pharmaceutical industry, Methanesulfonamide, N-(1,1-dimethylethyl)serves as an intermediate in the synthesis of various compounds, playing a crucial role in the development of new drugs and medicinal agents.
Used as an Antimicrobial Agent:
Methanesulfonamide, N-(1,1-dimethylethyl)is known for its antibiotic properties and is sometimes used as an antimicrobial agent in pharmaceutical preparations, helping to combat microbial infections.
Used as a Solvent:
Methanesulfonamide, N-(1,1-dimethylethyl)is also utilized as a solvent in various chemical processes, taking advantage of its solubility properties to dissolve other substances and facilitate reactions.
Safety Precautions:
It is important to handle Methanesulfonamide, N-(1,1-dimethylethyl)with care, as it may be harmful if ingested, inhaled, or comes into contact with the skin. Proper safety measures should be taken during its use to minimize potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 2512-23-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,1 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2512-23:
(6*2)+(5*5)+(4*1)+(3*2)+(2*2)+(1*3)=54
54 % 10 = 4
So 2512-23-4 is a valid CAS Registry Number.
2512-23-4Relevant academic research and scientific papers
N-Phosphonoyl and N-Phosphoroyl Hydroxylamines: Reactions of their O-Sulphonyl Derivatives with t-Butylamine
Harger, Martin J. P.,Smith, Adrian
, p. 2651 - 2656 (2007/10/02)
The N-phosphonoylhydroxylamines Ph(ArO)P(O)NHOH (Ar = p-chlorophenyl or p-tolyl) and the N-phosphoroylhydroxylamines (ArO)2P(O)NHOH (Ar = p-chlorophenyl or p-tolyl) have been prepared and converted into their O-methanesulphonyl and O-p-nitrobenzenesulphonyl derivatives.In the reactions of the sulphonyl derivatives with t-butylamine, the phosphonoyl compounds undergo a Lossen-like rearrangement with migration of the phenyl group from phosphorus to nitrogen.The phosphoroyl compounds do not rearrange with t-butylamine but give products that include (ArO)2P(O)NH2 and (ArO)2P(O)NHNHBut.
