152495-79-9 Usage
Uses
Used in Pharmaceutical Industry:
(R)-N-(tetrahydrofuran-3-yl)benzamide is used as a building block in organic synthesis for its potential in drug development. Its unique structure and properties make it a valuable tool for chemists and researchers working in the field of medicinal chemistry, facilitating the creation of new pharmaceutical compounds with specific therapeutic targets.
Used in Medicinal Chemistry Research:
(R)-N-(tetrahydrofuran-3-yl)benzamide is used as a research tool in medicinal chemistry for exploring its interactions with biological targets. Its chiral nature and specific arrangement of atoms contribute to its potential in various biological studies and drug discovery efforts, aiding in the understanding of its therapeutic effects and mechanisms of action.
Used in Drug Discovery:
(R)-N-(tetrahydrofuran-3-yl)benzamide is employed as a starting material in drug discovery for its potential to be modified and optimized to create new pharmaceutical agents. Its unique structural features allow for the development of compounds with specific binding affinities and selectivity towards molecular targets, which is essential for the treatment of various diseases and conditions.
Used in Other Industrial and Scientific Areas:
While primarily recognized in the pharmaceutical industry, (R)-N-(tetrahydrofuran-3-yl)benzamide may also have potential applications in other fields. Its unique properties could be harnessed in areas such as materials science, where it might contribute to the development of new materials with specific properties, or in chemical research, where it could be used to study reaction mechanisms and catalysis.
Check Digit Verification of cas no
The CAS Registry Mumber 152495-79-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,4,9 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 152495-79:
(8*1)+(7*5)+(6*2)+(5*4)+(4*9)+(3*5)+(2*7)+(1*9)=149
149 % 10 = 9
So 152495-79-9 is a valid CAS Registry Number.
152495-79-9Relevant academic research and scientific papers
Expeditious novel routes to enantiopure 3-amino tetrahydrofuran hydrochloride
Ramanujam, Rajendran,Ganjihal, Savita,Kalyanam, Nagabushanam,Majeed, Muhammed
, p. 663 - 668 (2013/07/11)
The synthesis of chemically and enantiomerically pure (S)-3-amino tetrahydrofuran hydrochloride starting from the natural amino acids, l-aspartic acid or l-methionine is described. The process involves no chromatography and can be easily carried out on a large scale. The enantiopurity of the final product was established by NMR and chiral HPLC methods.
Processes for the Manufacture of Chiral and Racemic Forms of 3-Aminotetrahydrofurans, Their Salts and Derivatives
-
Page/Page column 3, (2008/12/04)
A novel process for the synthesis of (S)-3-Amino-tetrahydrofuran and (R)-3-Amino-tetrahydrofuran is described. The process is applicable for substituted chiral-3-aminotetrahydrofuran derivatives.
A Remarkable Base-Induced Rearrangement of Hydroxy Oxazolines to Amido Tetrahydrofurans
Wilson, Kenneth J.,Sabat, Michal,McGarvey, Glenn J.
, p. 6180 - 6181 (2007/10/02)
Asymmetric β-hydroxy oxazolines heve been shown to rearrange at room temperature to isomeric tetrahydrofurans when deprotonated with potassium hydride in tetrahydrofuran.
