31197-69-0 Usage
Uses
Used in Organic Synthesis:
ETHYL 2-CYCLOHEXYL-2-HYDROXY-PHENYLACETATE is used as a key intermediate in the synthesis of various organic compounds. Its unique structure and properties allow it to be a versatile building block in the development of new molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, ETHYL 2-CYCLOHEXYL-2-HYDROXY-PHENYLACETATE is used as a starting material for the development of new drugs. Its chemical properties make it suitable for the synthesis of complex molecules with potential therapeutic effects.
Used in Chemical Research:
ETHYL 2-CYCLOHEXYL-2-HYDROXY-PHENYLACETATE is also used in chemical research as a model compound to study various reaction mechanisms and to develop new synthetic methodologies. This helps researchers gain a deeper understanding of chemical processes and improve the efficiency of organic synthesis.
Used in Flavor and Fragrance Industry:
Due to its unique chemical structure, ETHYL 2-CYCLOHEXYL-2-HYDROXY-PHENYLACETATE can be used as a component in the creation of new fragrances and flavors. Its light yellow oil form and distinct properties make it a valuable addition to the flavor and fragrance industry.
Check Digit Verification of cas no
The CAS Registry Mumber 31197-69-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,1,9 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 31197-69:
(7*3)+(6*1)+(5*1)+(4*9)+(3*7)+(2*6)+(1*9)=110
110 % 10 = 0
So 31197-69-0 is a valid CAS Registry Number.
31197-69-0Relevant academic research and scientific papers
OLIGOMER-ANTICHOLINERGIC AGENT CONJUGATES
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Page/Page column 37, (2008/12/07)
The invention provides anticholinergic agents that are chemically modified by covalent attachment of a water-soluble oligomer. A conjugate of the invention, when administered by any of a number of administration routes, exhibits characteristics that are different as compared to the characteristics of the anticholinergic agent not attached to the water-soluble oligomer.
Synthesis and optimization of novel and selective muscarinic M3 receptor antagonists
Kumar, Naresh,Kaur, Kirandeep,Aeron, Shelly,Dharmarajan, Sankaranarayanan,Silamkoti, Arun D.V.,Mehta, Anita,Gupta, Suman,Chugh, Anita,Gupta, Jang B.,Salman, Mohammad,Palle, Venkata P.,Cliffe, Ian A.
, p. 5256 - 5260 (2008/02/11)
A series of constrained piperidine analogues were synthesized as novel muscarinic M3 receptor antagonists. Evaluation of these compounds in binding assays revealed that they not only have high affinity for the M3 receptor but also have high selectivity over the M2 receptor.
Ethyl Mandelate as a Convenient New Benzoyl Anion Equivalent
Aitken, R. Alan,Thomas, Andrew W.
, p. 293 - 294 (2007/10/03)
Ethyl mandelate acts as a convenient benzoyl anion equivalent for the formation of alkyl aryl ketones by deprotonation-alkylation followed by flash vacuum pyrolysis.
