792886-64-7 Usage
Uses
Used in the Production of Polyurethane Foam:
(R)-2-isopropylmorpholine is used as a catalyst in the production of polyurethane foam, a versatile material with applications in furniture, bedding, automotive, and construction industries. Its catalytic properties facilitate the reaction process, leading to the formation of the desired foam structure.
Used in Pharmaceutical Synthesis:
(R)-2-isopropylmorpholine is used as a building block in the synthesis of various pharmaceuticals. Its unique structure and reactivity make it a valuable component in the development of new drugs, contributing to the advancement of medical treatments.
Used in Agrochemical Synthesis:
(R)-2-isopropylmorpholine is also utilized as a building block in the synthesis of agrochemicals, which are essential for crop protection and enhancement of agricultural productivity. Its role in the development of these chemicals helps improve crop yields and protect against pests and diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 792886-64-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,2,8,8 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 792886-64:
(8*7)+(7*9)+(6*2)+(5*8)+(4*8)+(3*6)+(2*6)+(1*4)=237
237 % 10 = 7
So 792886-64-7 is a valid CAS Registry Number.
792886-64-7Relevant academic research and scientific papers
Diastereoselective synthesis of enantiopure morphelines by electrophilic selenium-induced 6-exo cyclizations on chiral 3-allyl-2-hydroxymethylperhydro-1, 3-benzoxazine derivatives
Pedrosa, Rafael,Andres, Celia,Mendiguchia, Pilar,Nieto, Javier
, p. 8854 - 8863 (2007/10/03)
Enantiopure morpholine derivatives have been prepared by selenocyclofunctionalization of chiral 3-allyl-2-hydroxymethyl-substituted perhydro-1,3-benzoxazine derivatives. The cyclization occurs in high yields and diastereoselection, although the temperature of the reaction and the structure of the substituent at C-2 and the substitution pattern of the double bond can modify the regio- and stereochemistry of the final products.
