91271-58-8 Usage
Uses
Used in Pharmaceutical Synthesis:
[2-(pyrrolidin-1-ylmethyl)phenyl]methanol is utilized as an intermediate in the production of various pharmaceutical drugs. Its unique structure allows it to be a key component in the synthesis of a range of medicinal compounds, contributing to the development of new treatments and therapies.
Used as a Building Block in Organic Synthesis:
In the chemical industry, [2-(pyrrolidin-1-ylmethyl)phenyl]methanol serves as a building block in the synthesis of various bioactive molecules. Its ability to be incorporated into more complex organic structures makes it a valuable asset in creating molecules with specific biological activities.
Used as a Chiral Auxiliary in Asymmetric Synthesis:
Furthermore, [2-(pyrrolidin-1-ylmethyl)phenyl]methanol has potential applications as a chiral auxiliary in asymmetric synthesis. This role is crucial for the production of enantiomerically pure compounds, which are essential in many pharmaceutical applications where the effectiveness and safety of a drug can depend on its stereochemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 91271-58-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,2,7 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91271-58:
(7*9)+(6*1)+(5*2)+(4*7)+(3*1)+(2*5)+(1*8)=128
128 % 10 = 8
So 91271-58-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO/c14-10-12-6-2-1-5-11(12)9-13-7-3-4-8-13/h1-2,5-6,14H,3-4,7-10H2
91271-58-8Relevant academic research and scientific papers
O-Nucleophilic Amino Alcohol Acyl-Transfer Catalysts: The Effect of Acidity of the Hydroxyl Group on the Activity of the Catalyst
Wayman, Kjirsten A.,Sammakia, Tarek
, p. 4105 - 4108 (2007/10/03)
(Equation presented) Amino alcohol-derived acyl-transfer catalysts are shown to operate by an O-nucleophilic mechanism, and catalysts bearing electron-withdrawing groups in proximity to the hydroxyl group are found to be more active. This is attributed to
