323196-39-0 Usage
Uses
Used in Pharmaceutical Industry:
(1R,6R)-6-tert-butoxycarbonylamino-cyclohex-3-ene carboxylic acid methyl ester is used as an intermediate in the synthesis of pharmaceutical compounds for its unique stereochemistry and Boc-protected amine group. This feature allows for the development of new drugs with specific biological activities, potentially leading to more effective treatments for various diseases.
Used in Agrochemical Industry:
In the agrochemical field, (1R,6R)-6-tert-butoxycarbonylamino-cyclohex-3-ene carboxylic acid methyl ester is used as a building block for the creation of novel agrochemicals. Its chiral nature and Boc protection may contribute to the development of more targeted and environmentally friendly pesticides or herbicides, reducing the impact on non-target organisms and ecosystems.
Used in Organic Synthesis:
(1R,6R)-6-tert-butoxycarbonylamino-cyclohex-3-ene carboxylic acid methyl ester is utilized as a key intermediate in the preparation of complex organic molecules. Its unique structural features, including the Boc-protected amine and chiral centers, make it a valuable component in the synthesis of biologically active compounds, natural products, and other complex organic structures.
Check Digit Verification of cas no
The CAS Registry Mumber 323196-39-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,3,1,9 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 323196-39:
(8*3)+(7*2)+(6*3)+(5*1)+(4*9)+(3*6)+(2*3)+(1*9)=130
130 % 10 = 0
So 323196-39-0 is a valid CAS Registry Number.
323196-39-0Relevant academic research and scientific papers
2-Azidoethoxy derivatives of 2-aminocyclohexanecarboxylic acids (ACHC): Interesting building blocks for the synthesis of cyclic β-peptide conjugates
Reina, Jose J.,Bernardi, Anna
experimental part, p. 5770 - 5775 (2011/09/12)
Oligomers of cyclic-β-aminoacids possess a high resistance to peptidase-catalyzed hydrolysis and display a high intrinsic tendency to adopt regular secondary structures. These characteristics are attractive to develop new biologically active substances. H
Diels-Alder approaches to ring-functionalized cyclic β-amino acids
Wipf,Wang
, p. 8747 - 8751 (2007/10/03)
Catalytic asymmetric Diels-Alder reactions with aminodiene 1 and desymmetrized fumarate 8 were used for efficient access to dihydroxylated cis- and trans-aminocyclohexane β-amino acids. (C) 2000 Elsevier Science Ltd.
