67928-34-1 Usage
Uses
Used in Pharmaceutical Synthesis:
(S)-N-(p-Methoxybenzylidene)-2-amino-1-propanol is used as a key component in the synthesis of various pharmaceuticals for [application reason]. Its unique structure allows for the creation of new drugs with specific therapeutic properties.
Used as a Chiral Intermediate:
In the chemical industry, (S)-N-(p-Methoxybenzylidene)-2-amino-1-propanol is used as a chiral intermediate for [application reason]. Its specific stereochemistry is crucial in the development of enantiomerically pure compounds, which are essential in the pharmaceutical and agrochemical sectors.
Used in the Production of Optical Materials:
(S)-N-(p-Methoxybenzylidene)-2-amino-1-propanol is also utilized in the production of optical materials for [application reason]. Its optical properties make it suitable for applications in the field of optoelectronics and display technologies.
Used in Research and Development:
In the field of research and development, (S)-N-(p-Methoxybenzylidene)-2-amino-1-propanol is used as a model compound for [application reason]. Its complex structure provides insights into the behavior of similar compounds and aids in the development of new synthetic methods and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 67928-34-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,9,2 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 67928-34:
(7*6)+(6*7)+(5*9)+(4*2)+(3*8)+(2*3)+(1*4)=171
171 % 10 = 1
So 67928-34-1 is a valid CAS Registry Number.
67928-34-1Relevant articles and documents
Use of Liquid Crystal Induced Circular Dichroism for Absolute Configurational Assignments of β-Amino Alcohols
Rinaldi, Peter L.,Wilk, Melody
, p. 2141 - 2146 (2007/10/02)
Dissolution of small quantities of chiral β-amino alcohols in liquid crystalline N-(p-methoxybenzylidene)-p-n-butylaniline (MBBA) results in induced rotations due to the formation of a cholesteric (chiral) liquid crystal phase.The induced rotations are several orders of magnitude larger than those observed for β-amino alcohols in isotropic solutions, and the signs of these rotations can be correlated with the absolute configurations of the chiral amino alcohols when standard conformational analysis arguments and the preference of elongated molecules to align with MBBA are considered.