80575-79-7 Usage
Uses
Used in Organic Synthesis:
[S-(R,R)]-[1-[(Methoxyamino)carbonyl]-2-[(methylsulfonyl)oxy]propyl]-carbamic Acid 1,1-Dimethylethyl Ester is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure and functional groups make it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [S-(R,R)]-[1-[(Methoxyamino)carbonyl]-2-[(methylsulfonyl)oxy]propyl]-carbamic Acid 1,1-Dimethylethyl Ester is used as a key component in the development of new drugs. Its versatile chemical properties allow it to be incorporated into a wide range of drug candidates, potentially leading to the discovery of novel therapeutic agents.
Used in Agrochemical Industry:
[S-(R,R)]-[1-[(Methoxyamino)carbonyl]-2-[(methylsulfonyl)oxy]propyl]-carbamic Acid 1,1-Dimethylethyl Ester is also utilized in the agrochemical sector for the synthesis of new pesticides and herbicides. Its ability to form stable derivatives with various agrochemical active ingredients makes it a promising candidate for the development of more effective and environmentally friendly products.
Used in Specialty Chemicals:
In the specialty chemicals market, [S-(R,R)]-[1-[(Methoxyamino)carbonyl]-2-[(methylsulfonyl)oxy]propyl]-carbamic Acid 1,1-Dimethylethyl Ester is employed as a raw material for the production of high-value chemicals. Its unique properties and reactivity enable the creation of innovative products with specific applications in various industries, such as coatings, adhesives, and polymers.
Check Digit Verification of cas no
The CAS Registry Mumber 80575-79-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,5,7 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 80575-79:
(7*8)+(6*0)+(5*5)+(4*7)+(3*5)+(2*7)+(1*9)=147
147 % 10 = 7
So 80575-79-7 is a valid CAS Registry Number.
80575-79-7Relevant academic research and scientific papers
Monobactams. Preparation of (S)-3-Amino-2-oxoazetidine-1-sulfonic Acids from L-α-Amino-β-hydroxy Acids via Their Hydroxamic Esters
Floyd, David M.,Fritz, Alan W.,Pluscec, Josip,Weaver, Eugene R.,Cimarusti, Christopher M.
, p. 5160 - 5167 (2007/10/02)
The cyclization of the O-methylhydroxamates 13-15 afforded excellent yields of the 1-methoxyazetidinones 16-18.Reductive cleavage of the methoxy group gave N-1-unsubstituted azetidinones 9, 19, and 20 which were sulfonated and deprotected, yielding zwitterions 29-31.These materials serve as general intermediates for the preparation of a large variety of monobactam antimicrobial agents.
