112297-89-9 Usage
Type
Chiral ketone compound
Usage
Used in the synthesis of pharmaceuticals and agrochemicals, key intermediate in the preparation of various biologically active compounds, commonly used as a reagent in organic chemistry reactions
Physical form
Colorless liquid
Molecular weight
332.505 g/mol
Reactivity
High reactivity
Importance
Used as a building block in the production of various chiral compounds, making it an important chemical in the field of organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 112297-89-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,2,9 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 112297-89:
(8*1)+(7*1)+(6*2)+(5*2)+(4*9)+(3*7)+(2*8)+(1*9)=119
119 % 10 = 9
So 112297-89-9 is a valid CAS Registry Number.
112297-89-9Relevant articles and documents
Cleavage of Carbon-Carbon Bonds with High Stereochemical Control. 6. Asymmetric Synthesis of Chiral C-Centered Organosilanes by Haller-Bauer Cleavage of Optically Active, Nonenolizable α-Silyl Phenyl Ketones
Gilday, John P.,Gallucci, Judith C.,Paquette, Leo A.
, p. 1399 - 1408 (2007/10/02)
Sequential alkylation and methylation of l-menthyl ester 10 provides diastereomeric mixtures in which 12 is slighthly enhanced over 13.Conversely, C-silation and alkylation of propionate ester 11 delivers 13 in excess.In either cause, a single chromatogra
