588683-09-4 Usage
Uses
Used in Pharmaceutical Industry:
(2R)-2-AMINO-2-(2-FURYL)ETHAN-1-OL is used as a chiral building block for the synthesis of various pharmaceuticals and biologically active compounds. Its unique structure allows for the creation of enantiomerically pure molecules, which is crucial for the development of effective and safe drugs.
Used in Asymmetric Catalysis:
(2R)-2-AMINO-2-(2-FURYL)ETHAN-1-OL has shown potential as a chiral ligand in asymmetric catalysis. This application is significant in the synthesis of enantiomerically pure compounds, which are essential in various chemical and pharmaceutical processes.
Used in Organic Chemistry Research:
Due to its furan ring and amino group, (2R)-2-AMINO-2-(2-FURYL)ETHAN-1-OL serves as a valuable starting material for research in organic chemistry. It can be used to explore new reactions, mechanisms, and the synthesis of novel organic compounds with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 588683-09-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,8,6,8 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 588683-09:
(8*5)+(7*8)+(6*8)+(5*6)+(4*8)+(3*3)+(2*0)+(1*9)=224
224 % 10 = 4
So 588683-09-4 is a valid CAS Registry Number.
588683-09-4Relevant academic research and scientific papers
Cong, Xin,Liu, Ke-Gang,Liao, Qing-Jiang,Yao, Zhu-Jun
, p. 8567 - 8571 (2005)
Zinc-mediated propargylation of α-acylaminoaldehydes, and subsequent oxidative isomerization followed by Ag(I)-catalyzed cycloisomerization conveniently provides a new enantioselective route to the corresponding 2-aminoalkylfurans. One of these furans was
Enantioselective synthesis of both enantiomers of 2-amino-2-(2-furyl)ethan-1-ol as a flexible building block for the preparation of serine and azasugars
Demir, Ayhan S.,Sesenoglu, Oezge,Aksoy-Cam, Hilal,Kaya, Handan,Aydogan, Kenan
, p. 1335 - 1340 (2007/10/03)
The selective conversion of 1-(2-furyl)-2-hydroxyethan-1-one and ethyl 2-(2-furyl)-2-oxo acetate into (E)- and (Z)-oximes and oxime ethers followed by oxazaborolidine-catalyzed enantioselective reduction using different amino alcohols furnished both enantiomers of the important chiral building block 2-amino-2-(2-furyl)ethan-1-ol with an ee of up to 96%.
