77472-23-2 Usage
Description
4,4-dimethyl-2-(propan-2-yl)-1,3-oxazolidine is a heterocyclic organic compound with the molecular formula C7H15NO. It features a five-membered ring containing oxygen and nitrogen atoms, and is known for its applications in various chemical processes due to its unique structure and properties.
Uses
Used in Pharmaceutical Industry:
4,4-dimethyl-2-(propan-2-yl)-1,3-oxazolidine serves as a chiral auxiliary in asymmetric synthesis, which is crucial for controlling the stereochemistry of reactions. This role is vital in the production of enantiomerically pure pharmaceuticals, ensuring the desired biological activity and minimizing potential side effects.
Used in Fine Chemicals Synthesis:
As a building block, 4,4-dimethyl-2-(propan-2-yl)-1,3-oxazolidine contributes to the synthesis of various fine chemicals. Its structural characteristics make it a valuable component in creating complex organic molecules with specific properties for use in different industries.
Used in Polymer and Material Science:
4,4-dimethyl-2-(propan-2-yl)-1,3-oxazolidine also finds applications in the production of polymers and materials. Its incorporation can lead to the development of new materials with improved properties, such as enhanced stability, reactivity, or selectivity in various applications.
With its low toxicity and relative safety for handling and use, 4,4-dimethyl-2-(propan-2-yl)-1,3-oxazolidine is a preferred choice in chemical processes where safety and environmental impact are concerns.
Check Digit Verification of cas no
The CAS Registry Mumber 77472-23-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,7 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 77472-23:
(7*7)+(6*7)+(5*4)+(4*7)+(3*2)+(2*2)+(1*3)=152
152 % 10 = 2
So 77472-23-2 is a valid CAS Registry Number.
77472-23-2Relevant articles and documents
Reaction of β-iminoalcohols with sulfur dioxide. Synthesis of (±)-(2-hydroxyalkylamino)phenyl(isopropyl)-methanesulfonic acids
Gryaznov,Kataeva,Naumova,Musin,Al'fonsov
experimental part, p. 761 - 764 (2011/01/07)
Reactions of 2-(N-isopropylidene)amino-2-methylpropanol, 2-(N-benzylidene)-, and 2-(N-isopro-pylidene)aminoethanols with sulfur dioxide in aqueous ethanol medium produce (±)-(2-hydroxyalkylamino)- phenyl(isopropyl)methanesulfonic acids. Structure of (±)-(
