159752-38-2 Usage
Chemical compound
A complex molecule used in organic synthesis as a catalyst for various chemical reactions.
Chiral Lewis acid
A type of molecule that has a non-superimposable mirror image and can act as a catalyst in chemical reactions.
Asymmetric reduction of prochiral ketones
The compound is used to selectively reduce prochiral ketones to produce chiral alcohols, which are important in the synthesis of pharmaceuticals and other chiral molecules.
Enantioselective reduction of aromatic ketones
The compound efficiently catalyzes the enantioselective reduction of aromatic ketones, providing high enantioselectivity and yield.
Potential in other asymmetric reactions
The compound has demonstrated potential as a catalyst in other types of asymmetric reactions, making it a valuable tool in the field of organic chemistry and drug discovery.
Structure
The compound has a complex structure with a 1,3,2-oxazaborolidine core, a 2-[2-(1-methoxyethyl)phenyl] group, and a 3,4-dimethyl-5-phenyl substituent.
Applications
The compound is used in the synthesis of various chiral molecules, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Importance
The compound is a valuable tool in the field of organic chemistry and drug discovery due to its ability to catalyze a wide range of asymmetric reactions with high enantioselectivity and yield.
Check Digit Verification of cas no
The CAS Registry Mumber 159752-38-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,7,5 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 159752-38:
(8*1)+(7*5)+(6*9)+(5*7)+(4*5)+(3*2)+(2*3)+(1*8)=172
172 % 10 = 2
So 159752-38-2 is a valid CAS Registry Number.
