5339-01-5 Usage
Description
3-DIMETHYLAMINOPHENYLMETHYLCARBINOL is a chemical compound characterized by the molecular formula C11H17NO. It features a tertiary amine with a hydroxyl group attached to a benzene ring, which is substituted with two methyl groups and one dimethylamine group. 3-DIMETHYLAMINOPHENYLMETHYLCARBINOL is recognized for its role as a chiral auxiliary in organic synthesis and for its potential therapeutic properties, including anti-inflammatory and anti-nociceptive effects.
Uses
Used in Organic Synthesis:
3-DIMETHYLAMINOPHENYLMETHYLCARBINOL is utilized as a chiral auxiliary, playing a crucial role in asymmetric synthesis. Its unique structure aids in the selective formation of enantiomers, which is vital for producing biologically active compounds with desired properties.
Used in Pharmaceutical Development:
Due to its anti-inflammatory and anti-nociceptive effects, 3-DIMETHYLAMINOPHENYLMETHYLCARBINOL holds promise for potential pharmaceutical applications. It may be developed into new drugs targeting inflammation and pain, contributing to the advancement of treatments for various conditions.
Used in the Preparation of Chiral Alcohols:
3-DIMETHYLAMINOPHENYLMETHYLCARBINOL also serves as a reagent for the preparation of chiral alcohols, which are essential building blocks in the synthesis of pharmaceuticals and other biologically relevant molecules. Its use in this capacity underscores its importance in the field of organic chemistry and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 5339-01-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5339-01:
(6*5)+(5*3)+(4*3)+(3*9)+(2*0)+(1*1)=85
85 % 10 = 5
So 5339-01-5 is a valid CAS Registry Number.
5339-01-5Relevant articles and documents
Photochemical Reaction of N,N-Dimethylanilines with N-Substituted Maleimides Utilizing Benzaldehyde as the Photoinitiator
Nikitas, Nikolaos F.,Theodoropoulou, Maria A.,Kokotos, Christoforos G.
supporting information, p. 1168 - 1173 (2021/02/01)
Photoorganocatalysis constitutes a powerful domain of photochemistry and organic synthesis. The scaffold of pyrrolo[3,4-c]quinolinoles exhibits interesting and potent inhibition against various enzymes, making them really promising pharmaceutical targets. Herein, we describe a photochemical methodology for the reaction of N,N-dimethylanilines with N-substituted maleimides, utilizing benzaldehyde as the photoinitiator. A variety of substituted N,N-dimethylanilines and N-substituted maleimides were converted into the corresponding adducts in moderate to high yields.
