115146-09-3 Usage
Description
(+/-)-N-(trans-2-hydroxy-indan-1-yl)-acetamide is a chiral chemical compound with a molecular formula of C11H13NO2. It is an acetamide derivative featuring a 2-hydroxy-indan-1-yl substituent, and it exists as a mixture of both enantiomers. (+/-)-N-(trans-2-hydroxy-indan-1-yl)-acetamide is frequently utilized as a building block in the synthesis of pharmaceuticals and biologically active compounds, with its applications varying depending on the specific enantiomer or derivative.
Uses
Used in Pharmaceutical Synthesis:
(+/-)-N-(trans-2-hydroxy-indan-1-yl)-acetamide is used as a key building block for the synthesis of various pharmaceuticals and biologically active compounds. Its unique structure and functional groups make it a valuable component in the development of new drugs and therapeutic agents.
Used in Research and Development:
In the field of research and development, (+/-)-N-(trans-2-hydroxy-indan-1-yl)-acetamide serves as a versatile compound for exploring its potential applications and properties. Scientists and researchers use it to investigate its interactions with biological targets and to develop novel derivatives with improved pharmacological profiles.
Used in Chiral Chemistry:
Due to its chiral nature, (+/-)-N-(trans-2-hydroxy-indan-1-yl)-acetamide is also used in chiral chemistry to study the effects of stereochemistry on the biological activity and pharmacokinetics of compounds. This knowledge can be crucial for optimizing the safety and efficacy of new drug candidates.
Used in Drug Design:
In the process of drug design, (+/-)-N-(trans-2-hydroxy-indan-1-yl)-acetamide is employed as a structural element to create new molecules with specific therapeutic targets. Its incorporation into drug candidates can lead to the development of more effective and selective medications.
Used in Chemical Libraries:
(+/-)-N-(trans-2-hydroxy-indan-1-yl)-acetamide is also utilized in the creation of chemical libraries for high-throughput screening. These libraries contain a vast array of diverse compounds, including chiral molecules like (+/-)-N-(trans-2-hydroxy-indan-1-yl)-acetamide, which can be screened against various biological targets to identify potential drug leads.
Used in Analytical Chemistry:
In analytical chemistry, (+/-)-N-(trans-2-hydroxy-indan-1-yl)-acetamide can be employed as a reference compound for the development and validation of analytical methods, such as chiral chromatography and spectroscopy. This helps in the accurate determination of enantiomeric purity and the study of stereoselective processes in chemical and biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 115146-09-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,1,4 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 115146-09:
(8*1)+(7*1)+(6*5)+(5*1)+(4*4)+(3*6)+(2*0)+(1*9)=93
93 % 10 = 3
So 115146-09-3 is a valid CAS Registry Number.
115146-09-3Relevant articles and documents
The Bahavior of Indene Oxide in the Ritter Reaction: A Simple Route to cis-Aminoindanol
Senanayake, Chris H.,Roberts, F. Edward,DiMichele, Lisa M.,Ryan, Kenneth M.,Liu, Ji,et al.
, p. 3993 - 3996 (1995)
A regio- and stereoselective synthesis of cis-1-aminoindan-2-ol via a Ritter reaction is described.
