756486-11-0 Usage
Uses
Used in Organic Chemistry:
(2S,4R)-4-[(tert-butoxycarbonyl)amino]-1-(9-fluorenylmethoxycarbonyl)piperidine-2-carboxylic acid is used as a synthetic intermediate for the creation of more complex organic molecules. Its unique structure, including the piperidine ring and carboxylic acid, along with the protective groups, makes it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, (2S,4R)-4-[(tert-butoxycarbonyl)amino]-1-(9-fluorenylmethoxycarbonyl)piperidine-2-carboxylic acid is used as a key building block for the development of new drugs. Its structural features allow for the creation of diverse medicinal compounds with potential therapeutic applications.
Used in Agrochemical Development:
(2S,4R)-4-[(tert-butoxycarbonyl)amino]-1-(9-fluorenylmethoxycarbonyl)piperidine-2-carboxylic acid is also utilized in the agrochemical sector as a precursor for the synthesis of novel pesticides and other crop protection agents. Its versatility in organic synthesis contributes to the development of innovative products designed to enhance crop yield and quality.
Used in Specialty Chemicals Production:
(2S,4R)-4-[(tert-butoxycarbonyl)amino]-1-(9-fluorenylmethoxycarbonyl)piperidine-2-carboxylic acid finds application in the production of specialty chemicals, where its unique structural elements can be leveraged to create high-value products for various industries, such as materials science, coatings, and adhesives. The protective groups present in the molecule ensure that it can be efficiently incorporated into these complex formulations without unwanted side reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 756486-11-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,6,4,8 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 756486-11:
(8*7)+(7*5)+(6*6)+(5*4)+(4*8)+(3*6)+(2*1)+(1*1)=200
200 % 10 = 0
So 756486-11-0 is a valid CAS Registry Number.
756486-11-0Relevant academic research and scientific papers
Synthesis of free and Nα-Fmoc-/Nγ-Boc- protected (2S,4S)- and (2S,4R)-4-aminopipecolic acids
Machetti, Fabrizio,Cordero, Franca M.,De Sarlo, Francesco,Papini, Anna M.,Alcaro, Maria C.,Brandi, Alberto
, p. 2928 - 2935 (2007/10/03)
The preparation of (2S,4S)- and (2S,4R)-4-aminopipecolic acid, a conformationally constrained basic amino acid bearing orthogonal N α/Nγ-protection suitable for solid-phase peptide synthesis, is reported. These amino acids were synthesised from enantiopure ethyl (2S)-4-oxo-1-(1-phenylethyl)-piperidine-2-carboxylate (1) with introduction of the side-chain amino group by reductive amination, followed by protection/deprotection of the functional groups. A mixture of Fmoc-Sly(Boc)-OH 6 and 7 was used to establish their compatibility in solid-phase peptide synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.
