130930-43-7 Usage
Uses
Used in Organic Synthesis:
(R)-1-AMINO-2,2-DIMETHYLCYCLOPROPANECARBOXYLIC ACID is used as a building block in organic synthesis for its unique chemical structure, which allows for a variety of chemical reactions and the creation of diverse compounds.
Used in Pharmaceutical Production:
(R)-1-AMINO-2,2-DIMETHYLCYCLOPROPANECARBOXYLIC ACID is used as a key component in the production of pharmaceuticals, leveraging its unique properties to develop new drugs and improve existing ones.
Used in Chemical Reactions:
(R)-1-AMINO-2,2-DIMETHYLCYCLOPROPANECARBOXYLIC ACID is used as a reactant in various chemical reactions, taking advantage of its specific orientation and functional groups to produce desired products.
Used in Industrial Processes:
(R)-1-AMINO-2,2-DIMETHYLCYCLOPROPANECARBOXYLIC ACID is utilized in different industrial processes, where its unique properties can enhance the efficiency and effectiveness of certain manufacturing techniques or contribute to the development of novel materials.
Check Digit Verification of cas no
The CAS Registry Mumber 130930-43-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,9,3 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 130930-43:
(8*1)+(7*3)+(6*0)+(5*9)+(4*3)+(3*0)+(2*4)+(1*3)=97
97 % 10 = 7
So 130930-43-7 is a valid CAS Registry Number.
130930-43-7Relevant academic research and scientific papers
Synthesis of (R)- and (S)-2,3-Methanovaline from (2S)-N-Benzoyl-2-tert-butyl-4-methylene-1,3-oxazolidin-5-one
Chinchilla, Rafael,Najera, Carmen,Garcia-Granda, Santiago,Menendez-Velazquez, Amador
, p. 5799 - 5802 (2007/10/02)
The reaction of (2S)-N-benzoyl-2-tert-butyl-4-methylene-1,3-oxazolidin-5-one (9) with isopropylidenetriphenylphosphorane at room temperature gives the corresponding cis and trans spirocyclopropane derivatives 10 in ca. 1:1 ratio.After separation of both diastereomers, by recrystallization and flasch chromatography, and further acid hydrolysis, enantiomerically pure (R)- and (S)-2,3-methanovaline 11 are obtained.
