153390-68-2 Usage
Description
2-(2,3-diMethoxyphenyl)propan-2-ol is an organic compound with the molecular formula C11H16O3. It is a colorless to pale yellow liquid with a distinct aromatic odor. 2-(2,3-diMethoxyphenyl)propan-2-ol is characterized by the presence of a phenyl ring with two methoxy groups at the 2nd and 3rd positions, and a propyl group attached to the 2nd carbon of the phenyl ring. Its chemical structure endows it with unique properties that make it suitable for various applications in different industries.
Uses
Used in Pharmaceutical Industry:
2-(2,3-diMethoxyphenyl)propan-2-ol is used as an intermediate for the synthesis of Miltirone (M344500), an active component in Salvia miltiorrhiza. Miltirone has demonstrated potential as a phytotherapeutic agent in the treatment of alcohol dependence. It works by inhibiting the increase in the abundance of the mRNA for the α4 subunit of the GABAA receptor induced by ethanol withdrawal in cultured hippocampal neurons, thus helping to alleviate the symptoms of alcohol withdrawal and reducing the risk of relapse.
Check Digit Verification of cas no
The CAS Registry Mumber 153390-68-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,3,9 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 153390-68:
(8*1)+(7*5)+(6*3)+(5*3)+(4*9)+(3*0)+(2*6)+(1*8)=132
132 % 10 = 2
So 153390-68-2 is a valid CAS Registry Number.
153390-68-2Relevant articles and documents
A three-step preparation of 3-isopropylcatechol
Majetich,Liu
, p. 2331 - 2335 (1993)
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Synthesis of [6,6,m]-Tricyclic Compounds via [4+2] Cycloaddition with Au or Cu Catalyst
Kang, Juyeon,Ham, Seunghwan,Seong, Chaehyeon,Oh, Chang Ho
supporting information, p. 1039 - 1043 (2021/05/05)
We synthesized [6,6,6]- and [6,6,7]-tricyclic compounds via intramolecular [4+2] cycloaddition by gold or copper catalysts. Substrates for cyclization were prepared by coupling reactions between eight types of diyne and four types of aromatic moieties. We have successfully synthesized eleven tricyclic compounds.
Convergent formal syntheses of (±)-brussonol and (±)-abrotanone via an intramolecular Marson-type cyclization
Martinez-Solorio, Dionicio,Jennings, Michael P.
supporting information; experimental part, p. 189 - 192 (2009/06/20)
The formal convergent syntheses of both (±)-brussonol and (±)-abrotanone are reported. The key step involved the diastereoselective capture of an in situ generated oxocarbenium cation via an intramolecular Friedel-Crafts/Marson-type cyclization.