192047-04-4 Usage
Uses
Used in Pharmaceutical Industry:
(1R,2S)-2-amino cyclohexanecarboxylic acid ethyl ester serves as a crucial building block in the synthesis of various pharmaceuticals. Its unique structure allows for the development of complex molecules with specific therapeutic properties, contributing to the advancement of new medications and treatments.
Used in Agrochemical Industry:
In the agrochemical sector, (1R,2S)-2-amino cyclohexanecarboxylic acid ethyl ester is utilized for the production of pesticides, herbicides, and other crop protection agents. Its reactivity and functionalization potential enable the creation of effective and targeted agrochemicals that can improve crop yields and protect against pests.
Used in Materials Science:
(1R,2S)-2-amino cyclohexanecarboxylic acid ethyl ester also finds applications in materials science, where it can be used to develop new materials with specific properties. Its ability to form complex molecules makes it suitable for creating materials with tailored characteristics for various applications, such as polymers, coatings, and adhesives.
Used in Organic Synthesis:
As a building block in organic synthesis, (1R,2S)-2-amino cyclohexanecarboxylic acid ethyl ester is employed in the synthesis of a wide range of organic compounds. Its versatile reactivity and potential for selective functionalization make it an essential component in the creation of complex organic molecules for various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 192047-04-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,0,4 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 192047-04:
(8*1)+(7*9)+(6*2)+(5*0)+(4*4)+(3*7)+(2*0)+(1*4)=124
124 % 10 = 4
So 192047-04-4 is a valid CAS Registry Number.
192047-04-4Relevant articles and documents
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
Approach to highly enantiopure β-amino acid esters by using lipase catalysis in organic media
Kanerva, Liisa T.,Csomos, Peter,Sundholm, Oskari,Bernath, Gabor,Fueloep, Ferenc
, p. 1705 - 1716 (2007/10/03)
Ethyl esters of ten alicyclic β-aminocarboxylic acids were resolved by lipase catalysis in organic solvents. The resolution was based on acylation of the amino group at the R-stereogenic centre with various 2,2,2- trifluoroethyl esters. An increase in the hydrophobic nature of the acyl donor enhanced the enantioselectivity and reactivity in the case of lipase SP 526 from Candida antarctica, while the opposite effect was observed with lipase PS from Pseudomonas cepacia. An unexceptional enantioselectivity enhancement was observed when 2,2,2-trifluoroethyl chloroacetate was used in the case of lipase PS catalysis.
