1226812-49-2 Usage
Uses
Used in Organic Synthesis:
(1R,6S)-6-(tert-butoxycarbonylamino)cyclohex-3-enecarboxylic acid is used as a building block for the synthesis of more complex organic molecules. Its unique structure and functional groups make it a versatile component in the creation of various organic compounds.
Used in Medicinal Chemistry:
(1R,6S)-6-(tert-butoxycarbonylamino)cyclohex-3-enecarboxylic acid is used as a starting material or intermediate in the development of pharmaceuticals. Its specific stereochemistry and functional groups may contribute to the design and synthesis of new drugs with potential therapeutic applications.
Used in Research and Development:
(1R,6S)-6-(tert-butoxycarbonylamino)cyclohex-3-enecarboxylic acid is used as a subject of study in research and development to explore its properties, reactivity, and potential applications. This may include investigations into its chemical behavior, stability, and interactions with other molecules, as well as its potential use in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1226812-49-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,6,8,1 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1226812-49:
(9*1)+(8*2)+(7*2)+(6*6)+(5*8)+(4*1)+(3*2)+(2*4)+(1*9)=142
142 % 10 = 2
So 1226812-49-2 is a valid CAS Registry Number.
1226812-49-2Relevant academic research and scientific papers
Selective synthesis of new fluorinated alicyclic β-amino ester stereoisomers
Kiss, Lorand,Forro, Eniko,Fustero, Santos,Fueloep, Ferenc
scheme or table, p. 4993 - 5001 (2011/10/09)
New fluorinated alicyclic β-amino ester stereoisomers with a cyclohexene or cyclohexane skeleton were prepared from cis- or trans-2-aminocyclohex-3-enecarboxylic acids in five or six steps through a regio- and stereoselective hydroxylation and hydroxy-fluorine exchange. Fluorinated aminoester enantiomers were synthesized from enantiopure cis- or trans-2-aminocyclohexenecarboxylic acid (prepared byenzymatic resolution of the racemic substances). New fluorinated alicyclic β-amino ester stereoisomers with a cyclohexene or cyclohexane skeleton were prepared from cis-or trans-2-aminocyclohex-3-enecarboxylicacids in five or six steps. Copyright
