17159-83-0 Usage
General Description
(4-oxocyclohexyl)methyl 4-methylbenzenesulfonate is a chemical compound that is used in various industrial and pharmaceutical applications. It is a derivative of cyclohexanone and methylbenzenesulfonate, and is often used as a reagent in organic synthesis. (4-oxocyclohexyl)methyl 4-methylbenzenesulfonate is known for its ability to act as a protecting group for alcohols and amines in organic chemistry reactions. It is also used in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Additionally, it has been studied for its potential use in the development of new materials and drug delivery systems. Overall, (4-oxocyclohexyl)methyl 4-methylbenzenesulfonate is a versatile chemical with a wide range of applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 17159-83-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,5 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17159-83:
(7*1)+(6*7)+(5*1)+(4*5)+(3*9)+(2*8)+(1*3)=120
120 % 10 = 0
So 17159-83-0 is a valid CAS Registry Number.
17159-83-0Relevant articles and documents
COMPOUNDS FOR THE TREATMENT OF HIV
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Page/Page column 228; 229, (2013/03/26)
The invention provides compounds of formula (I): or a salt thereof as described herein. The invention also provides pharmaceutical compositions comprising a compound of formula (I), processes for preparing compounds of formula (I), intermediates useful for preparing compounds of formula I and therapeutic methods for treating a Retroviridae viral infection including an infection caused by the HIV virus.
A New Synthesis of Bicycloocta-2,4-diene and Its Cycloaddition Reactions with Dienophiles.
Yin, Tyze-Kuan,Lee, Jon Gun,Borden, Weston Thatcher
, p. 531 - 534 (2007/10/02)
Bicycloocta-2,4-diene (4) has been synthesized by a new, nine-step route, starting from 2--1,3-butadiene and acrolein.Diene (4) proved almost as unreactive toward Diels-Alder cycloadditions as the previously studied 7,7-dimethy
