98288-60-9 Usage
Uses
Used in Organic Synthesis:
(2-Phenylsulfonyl)ethoxy Dichlorophosphine is utilized as a versatile reagent in organic synthesis, particularly for the preparation of phosphonates and phosphoramidates. Its unique structure allows for a wide range of applications in creating complex organic molecules.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, (2-Phenylsulfonyl)ethoxy Dichlorophosphine is employed as a key intermediate in the synthesis of various drugs. Its reactivity and functional groups contribute to the development of new medicinal compounds with potential therapeutic benefits.
Used in Agrochemical Production:
Agrochemicals also benefit from the use of (2-Phenylsulfonyl)ethoxy Dichlorophosphine as it plays a role in the synthesis of pesticides and other agricultural chemicals. Its properties enable the creation of effective products for crop protection and enhancement of agricultural yields.
Used in the Synthesis of Fine Chemicals:
(2-Phenylsulfonyl)ethoxy Dichlorophosphine is also used in the production of fine chemicals, which are high-purity chemicals employed in various industries, including fragrances, dyes, and specialty chemicals. Its presence in these syntheses ensures the quality and performance of the final products.
Safety Note:
It is crucial to handle (2-Phenylsulfonyl)ethoxy Dichlorophosphine with care due to its toxic and potentially hazardous nature. Proper safety measures and precautions should be taken to minimize risks during its use in chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 98288-60-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,2,8 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 98288-60:
(7*9)+(6*8)+(5*2)+(4*8)+(3*8)+(2*6)+(1*0)=189
189 % 10 = 9
So 98288-60-9 is a valid CAS Registry Number.
98288-60-9Relevant academic research and scientific papers
Ar(alk)ylsulfonyl ethyl groups as phosphorus-protecting functions
Claesen, C. A. A.,Segers, R. P. A. M.,Tesser, G. I.
, p. 119 - 122 (2007/10/02)
Various 2-ethanols were prepared and subsequently converted into the corresponding phosphorodichloridites in almost quantitative yield via a convenient synthetic route.The versatility of the method, which obviates the necessity of a distillation step, is demonstrated by the preparation of other (Ar(alk)yl phosphorodichloridites, including the unstable benzyl phosphorodichloridite.
