17572-39-3 Usage
Description
Diethyl 4-hydroxy-4-methyl-6-oxo-2-phenylcyclohexane-1,3-dicarboxylate is a chemical compound with the molecular formula C19H24O6. It is a derivative of phenylcyclohexane-1,3-dicarboxylic acid, featuring a phenyl group, two ester groups, an oxo group, and a hydroxy group. diethyl 4-hydroxy-4-Methyl-6-oxo-2-phenylcyclohexane-1,3-dicarboxylate is commonly utilized in organic synthesis and pharmaceutical research due to its cyclohexane ring structure and carboxylate groups, which are prevalent in many bioactive compounds. Its ester groups also make it a valuable building block for the synthesis of more complex molecules. However, it is essential to handle this chemical substance with care and follow appropriate safety precautions.
Uses
Used in Organic Synthesis:
Diethyl 4-hydroxy-4-methyl-6-oxo-2-phenylcyclohexane-1,3-dicarboxylate is used as a building block in organic synthesis for the creation of more complex molecules. Its ester groups facilitate the synthesis process, making it a versatile component in the development of new organic compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, diethyl 4-hydroxy-4-methyl-6-oxo-2-phenylcyclohexane-1,3-dicarboxylate is used as a starting material or intermediate in drug development. Its cyclohexane ring structure and carboxylate groups are common motifs in bioactive compounds, which may contribute to the discovery of new therapeutic agents.
Used in Drug Development:
Due to its potential as a component of bioactive compounds, diethyl 4-hydroxy-4-methyl-6-oxo-2-phenylcyclohexane-1,3-dicarboxylate is used in drug development to explore its properties and applications in creating new pharmaceuticals. Its unique structure may offer novel therapeutic opportunities in various medical fields.
Check Digit Verification of cas no
The CAS Registry Mumber 17572-39-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,7 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17572-39:
(7*1)+(6*7)+(5*5)+(4*7)+(3*2)+(2*3)+(1*9)=123
123 % 10 = 3
So 17572-39-3 is a valid CAS Registry Number.
InChI:InChI=1/C19H24O6/c1-4-24-17(21)15-13(20)11-19(3,23)16(18(22)25-5-2)14(15)12-9-7-6-8-10-12/h6-10,14-16,23H,4-5,11H2,1-3H3
17572-39-3Relevant articles and documents
A detailed investigation into the one-pot cascade reaction of ethyl 3,9-dimethyl-7-phenyl-6H-dibenzo-[b,d]pyran-6-one-8-carboxylate with phenylhydrazine
Chen, Chao-Yue,Qiao, Yu,Zhang, Lei,Wang, Xin,Yang, Ting-Hai
, p. 4079 - 4089 (2020)
Abstract: When synthesizing cyclohexane-annulated pyrazolones from a cyclohexonedicarboxylate derivative with phenylhydrazine under the catalysis of sulfuric acid in the air, up to five products were finally obtained from the one-pot procedure. Among the
An efficient regioselective synthesis of functionalized biphenyls via sequential reactions of aromatic aldehydes and β-keto esters or ketones
Sharma, Anindra,Pandey, Jyoti,Tripathi
scheme or table, p. 1812 - 1816 (2009/07/19)
Knoevenagel/Michael/Aldol reactions of aromatic aldehydes and β-keto esters/ketones in a sequential manner yielded intermediate cyclohexanones in good yields. The latter, on oxidative aromatization with iodine, afforded functionalized biphenyls with at le
Microwave assisted rapid and efficient synthesis of 2,1-benzoisoxazoles
Rajanarendar,Rao, E. Kalyan,Karunakar
, p. 805 - 807 (2007/10/03)
A simple extremely fast and high yielding protocol has been developed for the synthesis of 2,1-benzisoxazoles under microwave irradiation.
