179601-38-8 Usage
Uses
Used in Pharmaceutical Industry:
Cyclohexanecarboxylic acid, 2-amino-, ethyl ester, (1S,2R)is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique stereochemistry and reactivity make it a valuable building block for the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, Cyclohexanecarboxylic acid, 2-amino-, ethyl ester, (1S,2R)is utilized as a precursor in the production of agrochemicals. Its ability to form stable and effective compounds makes it a crucial component in the development of pesticides, herbicides, and other agricultural chemicals that help protect crops and enhance agricultural productivity.
Used in Organic Synthesis:
Cyclohexanecarboxylic acid, 2-amino-, ethyl ester, (1S,2R)is employed as a versatile building block in organic synthesis. Its unique structure and reactivity allow chemists to create a wide range of compounds with diverse applications, including the development of new materials, catalysts, and other specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 179601-38-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,6,0 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 179601-38:
(8*1)+(7*7)+(6*9)+(5*6)+(4*0)+(3*1)+(2*3)+(1*8)=158
158 % 10 = 8
So 179601-38-8 is a valid CAS Registry Number.
179601-38-8Relevant academic research and scientific papers
Regio- and stereoselective reactions between cyclic Baylis-Hillman type adducts and N-nucleophiles and P-nucleophile
Krawczyk, Ewa,Owsianik, Krzysztof,Skowrońska, Aleksandra
, p. 1449 - 1457 (2007/10/03)
New important organic compounds multifunctionalized cyclic 6-membered and 7-membered allylic amines, azide and phosphonates have been obtained via regio- and diastereoselective reactions of cyclic Baylis-Hillman type adducts 1 with N-nucleophiles and P-nu
Stereoselective reduction of enantiopure β-enamino esters by hydride: A convenient synthesis of both enantiopure β-amino esters
Cimarelli, Cristina,Palmieri, Gianni
, p. 5557 - 5563 (2007/10/03)
The reduction of enantiopure β-enamino esters 1 with sodium triacetoxyborohydride in acetic acid is described. This occurs with good diastereo- and enantioselectivity to yield β-amino esters 2 and 3 (after hydrogenolysis of the N-chiral group). A model is
