99799-10-7 Usage
Uses
Used in Chemical Synthesis:
3-METHOXYCYCLOHEXANECARBOXYLIC ACID is used as a building block in the synthesis of various organic compounds. Its unique structure allows it to be a versatile intermediate for creating pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-METHOXYCYCLOHEXANECARBOXYLIC ACID is used as a key intermediate for the production of certain drugs. Its cyclohexane ring and functional groups can be further modified to create molecules with specific therapeutic properties.
Used in Flavor and Fragrance Industry:
3-METHOXYCYCLOHEXANECARBOXYLIC ACID can be used as a starting material for the development of novel fragrances and flavor compounds. Its ability to undergo various chemical transformations makes it suitable for creating complex and unique scents and tastes.
Used in Material Science:
In material science, 3-METHOXYCYCLOHEXANECARBOXYLIC ACID may be utilized in the development of new polymers and materials with specific properties. Its cyclohexane ring and carboxylic acid functionality can contribute to the formation of polymers with tailored characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 99799-10-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,7,9 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 99799-10:
(7*9)+(6*9)+(5*7)+(4*9)+(3*9)+(2*1)+(1*0)=217
217 % 10 = 7
So 99799-10-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O3/c1-11-7-4-2-3-6(5-7)8(9)10/h6-7H,2-5H2,1H3,(H,9,10)
99799-10-7Relevant articles and documents
Protecting Groups that can be Removed through Photochemical Electron Transfer: Mechanistic and Product Studies on Photosensitized Release of Carboxylates from Phenacyl Esters
Banerjee, Anamitro,Falvey, Daniel E.
, p. 6245 - 6251 (2007/10/03)
Photolysis of electron-donating photosensitizers in the presence of various phenacyl esters (PhCOCH2-OCOR) results in C-O bond scission leading to the formation of acetophenone (PhCOCH3) and the corresponding carboxylic acid (RCO2H). Preparative experiments showed that the carboxylic acids are generated in high or quantitative isolated yields. It is argued that this reaction is initiated by a photoinduced electron transfer from the excited state sensitizer to the phenacyl ester. The latter process forms the anion radical of the phenacyl ester which in turn undergoes rapid C-O bond scission leading to the phenacyl radical and the corresponding carboxylate anion. This mechanism is supported by the following observations. (1) The phenacyl esters quench fluorescence from the sensitizers. (2) Analysis of the redox potentials of the sensitizer excited states and the substrates shows that the proposed electron transfer step is exergonic by 15-20 kcal/mol. (3) The byproducts are indicative of the proposed ion radical intermediates. In particular N-methylaniline is detected when N4Y-dimethylaniline is used as a sensitizer. (4) Competing processes are observed in phenacyl esters whose acid components are themselves labile to single-electron transfer. For example, phenacyl 4-bromophenylacetate showed bromide elimination in competition with deprotection.
