74892-00-5 Usage
Uses
Used in Organic Synthesis:
2-(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethyl 4-methylbenzenesulfonate is used as a reagent in organic synthesis for the production of various chemical compounds. Its unique structure allows it to participate in a wide range of chemical reactions, making it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Chemical Reactions:
In the chemical industry, 2-(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethyl 4-methylbenzenesulfonate is used as a reagent in various chemical reactions. Its ability to participate in a broad range of reactions makes it a versatile compound for the synthesis of new materials and the modification of existing ones.
Used in Research and Development:
Due to its unique structural and chemical properties, 2-(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethyl 4-methylbenzenesulfonate is also used in research and development for the discovery and development of new chemical compounds and processes. Its versatility and reactivity make it a valuable tool for chemists and researchers in various fields.
Used in Pharmaceutical Industry:
2-(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethyl 4-methylbenzenesulfonate is used as an intermediate in the synthesis of pharmaceutical compounds. Its unique structure and reactivity make it a valuable building block for the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 2-(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethyl 4-methylbenzenesulfonate is used as an intermediate in the synthesis of agrochemicals, such as pesticides and herbicides. Its unique properties make it a valuable component in the development of new and effective agricultural products.
Used in Specialty Chemicals Industry:
2-(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethyl 4-methylbenzenesulfonate is used in the production of specialty chemicals, such as fragrances, dyes, and other high-value compounds. Its unique structure and reactivity make it a valuable component in the synthesis of these specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 74892-00-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,9 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 74892-00:
(7*7)+(6*4)+(5*8)+(4*9)+(3*2)+(2*0)+(1*0)=155
155 % 10 = 5
So 74892-00-5 is a valid CAS Registry Number.
74892-00-5Relevant academic research and scientific papers
Homolytic Displacement at Saturated Carbon: Part 5. Synthesis of Cyclopropylmethyl, Bicyclohex-2-yl, Bicyclohept-2-yl and Cyclohexanespirocycloprop-2-yl Sulphones from the Corresponding But-3-enylcobaloximes
Gupta, B. Dass,Das, Indira,Dixit, Vandana
, p. 2409 - 2446 (2007/10/02)
But-3-enylcobaloxime reacts with arenesulphonyl chlorides under thermal and photochemical conditions to give cyclopropylmethyl sulphones.The yields depend upon the reaction conditions used.Similar reactions of cyclopent-2-enylmethylcobaloxime and cyclohex-2-enylmethylcobaloximes under photochemical conditions form a mixture of cis and trans isomers of bicyclohex-2-yl and bicyclohept-2-yl sulphones in (50:50) and (70:30) isomeric ratios respectively.However, cyclohex-3-enylcobaloximes form only the trans-bicyclohex-2-yl sulphone.Exclusive formation of cycloalkanespirocycloprop-2-yl sulphones is observed in the reactions of 2-(cyclo alk-1-enyl)ethylcobaloximes with arenesulphonyl chlorides.The reactions are free radical in nature and are believed to take place by a chain mechanism.In the key step a homolytic attack of the RSO2 radical at the terminal (δ) carbon of the butenyl ligand leads to the cyclized product.The exact nature of the ring closure step is uncertain, as both concerted and stepwise mechanisms are possible.
Rearrangements of Pinane Derivatives. Part 91. 8,8-Dimethyltricyclo-2,5>nonan-2β-ol, a Tricyclic Pinane Derivative
Giddings, Rodney M.,Jones-Parry, Richard,Owen, Rawson,Whittaker, David
, p. 1525 - 1528 (2007/10/02)
Acetolysis of the toluene-p-sulphonate ester of 2-(2-hydroxyethyl)-6,6-dimethylbicyclohept-2-ene (nopol) (1; R = OH) gave a good yield of the acetate of the previously unknown tricyclic pinane derivative 8,8-dimethyltrycyclo2,5>n
