233772-37-7 Usage
Description
(S)-(-)-2-AMINO-3-METHYL-1,1-DIPHENYLBUTANE is an organic compound with a unique molecular structure featuring a chiral center, which results in two possible enantiomers: (S) and (R). (S)-(-)-2-AMINO-3-METHYL-1,1-DIPHENYLBUTANE is characterized by its amino and methyl groups, as well as its diphenylbutane backbone. It is known for its potential applications in various fields due to its distinct chemical properties.
Uses
Used in Pharmaceutical Industry:
(S)-(-)-2-AMINO-3-METHYL-1,1-DIPHENYLBUTANE is used as a chiral test compound for the enantio-separation of primary amines by supercritical fluid chromatography (SFC). This application is crucial in the pharmaceutical industry, as it allows for the separation and analysis of enantiomers, which can have different biological activities and effects on the body. The ability to distinguish between these enantiomers is essential for the development of safe and effective drugs.
Used in Analytical Chemistry:
In the field of analytical chemistry, (S)-(-)-2-AMINO-3-METHYL-1,1-DIPHENYLBUTANE serves as a valuable reference compound for the development and optimization of chiral separation techniques. (S)-(-)-2-AMINO-3-METHYL-1,1-DIPHENYLBUTANE can be used to test the efficiency and accuracy of various chromatographic methods, ensuring that they are capable of distinguishing between enantiomers with high precision.
Used in Research and Development:
(S)-(-)-2-AMINO-3-METHYL-1,1-DIPHENYLBUTANE is also utilized in research and development, particularly in the study of chiral molecules and their interactions with other compounds. (S)-(-)-2-AMINO-3-METHYL-1,1-DIPHENYLBUTANE can be used as a model system to investigate the effects of chirality on chemical reactivity, binding affinity, and other properties, contributing to a deeper understanding of the role of chirality in chemical and biological processes.
Check Digit Verification of cas no
The CAS Registry Mumber 233772-37-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,3,7,7 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 233772-37:
(8*2)+(7*3)+(6*3)+(5*7)+(4*7)+(3*2)+(2*3)+(1*7)=137
137 % 10 = 7
So 233772-37-7 is a valid CAS Registry Number.
InChI:InChI=1/C17H21N/c1-13(2)17(18)16(14-9-5-3-6-10-14)15-11-7-4-8-12-15/h3-13,16-17H,18H2,1-2H3/t17-/m0/s1
233772-37-7Relevant articles and documents
Asymmetric Synthesis of α-(Diarylmethyl) Alkyl Amines through Regioselective Lithiation of α-Diarylmethanes and the Diastereoselective Addition to Ellman's Imines
Reddy, Leleti Rajender,Kotturi, Sharadsrikar,Waman, Yogesh,Patel, Chirag,Danidharia, Megha,Shenoy, Rajesh
, p. 6573 - 6579 (2018)
A highly regio- and diastereoselective lithiation/addition of α-diarylmethanes to N-tert-butanesulfinylimines is reported. This methodology also affords the preparation of enantiomerically pure α-(diarylmethyl) alkyl amines bearing quaternary centers.
A short synthesis of (S)-α-(diphenylmethyl)alkyl amines from amino acids
O'Hagan, David,Tavasli, Mustafa
, p. 1189 - 1192 (2007/10/03)
A range of (S)-α-(diphenylmethyl)alkyl amines were prepared from the corresponding (S)-α-amino acid ester hydrochlorides. These amines were derived by direct hydrogenation of their precursor oxazolidinones.
