217799-18-3 Usage
Description
Cyclohexanecarboxylic acid, 2-amino-, methyl ester, (1S,2S)(9CI) is a chiral chemical compound that is a methyl ester derivative of 2-amino-cyclohexanecarboxylic acid. It is characterized by its colorless to pale yellow liquid form and its asymmetric carbon atoms, which give it a specific spatial arrangement of atoms. Cyclohexanecarboxylic acid, 2-amino-, methyl ester, (1S,2S)(9CI) has potential applications in pharmaceutical and medicinal fields, and may exhibit biological activity, making it a promising candidate for the development of new drugs or therapeutic agents. However, further research and testing are required to fully understand its potential uses and implications.
Uses
Used in Pharmaceutical Industry:
Cyclohexanecarboxylic acid, 2-amino-, methyl ester, (1S,2S)(9CI) is used as a chiral compound in the pharmaceutical industry for its potential applications in the development of new drugs or therapeutic agents. Its unique spatial arrangement of atoms and potential biological activity make it a valuable candidate for further research and exploration.
Used in Medicinal Applications:
In the field of medicine, Cyclohexanecarboxylic acid, 2-amino-, methyl ester, (1S,2S)(9CI) is utilized for its potential to contribute to the discovery and creation of novel therapeutic agents. Its chiral nature and possible biological properties could lead to advancements in treating various medical conditions, pending further investigation and validation.
Check Digit Verification of cas no
The CAS Registry Mumber 217799-18-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,7,7,9 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 217799-18:
(8*2)+(7*1)+(6*7)+(5*7)+(4*9)+(3*9)+(2*1)+(1*8)=173
173 % 10 = 3
So 217799-18-3 is a valid CAS Registry Number.
217799-18-3Relevant articles and documents
Pd-catalyzed asymmetric allylic aminations with aromatic amine nucleophiles using chiral diaminophosphine oxides: DIAPHOXs
Nemoto, Tetsuhiro,Tamura, Shinji,Sakamoto, Tatsurou,Hamada, Yasumasa
, p. 1751 - 1759 (2008/12/21)
Asymmetric allylic aminations with aromatic amine nucleophiles using Pd-DIAPHOX catalyst systems are described. The asymmetric allylic aminations of various allylic carbonates proceeded using 2-5 mol % of the catalyst and BSA, providing the corresponding
