114218-34-7 Usage
Appearance
Liquid
+ Boiling point
Not available as it is a liquid at room temperature
+ Melting point
Not applicable as it is a liquid
+ Density
Not available
+ Solubility
Not available
+ Reactivity
Reacts as a chiral auxiliary and resolving agent in organic synthesis
+ Stability
Stable under normal conditions
+ Functional groups
Hydroxyl, ether, phenoxy, and methanesulfonate groups are present
Uses
+ Chiral auxiliary in organic synthesis
+ Resolving agent for the separation of enantiomers
+ Production of pharmaceuticals, agrochemicals, and other fine chemicals
Mechanism of action
+ Selectively binds to and separates different enantiomers in a reaction mixture
+ Controls the stereochemistry of reactions to form desired chiral products.
Check Digit Verification of cas no
The CAS Registry Mumber 114218-34-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,2,1 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 114218-34:
(8*1)+(7*1)+(6*4)+(5*2)+(4*1)+(3*8)+(2*3)+(1*4)=87
87 % 10 = 7
So 114218-34-7 is a valid CAS Registry Number.
114218-34-7Relevant articles and documents
Method for the synthesis of pharmacologically active compounds and intermediates for such synthesis
-
, (2008/06/13)
A process for the preparation of an aryloxypropanolamine of the formula wherein Ar is a carbocyclic or heterocyclic aromatic group and R is an alkyl or substituted alkyl group having 1 to 6 carbon atoms, characterized in subjecting a compound of the formula STR1 to oxidative cleavage to a dialdehyde of the formula STR2 which is then made subject to reduction, amination, acetal hydrolysis, and, where required, removal of a nitrogen protective group, to the formation of a compound of formula I, or an acid addition salt thereof, a compound of formula II and the preparation thereof from mannitol.
