3770-22-7 Usage
Description
6-OXO-PIPERIDINE-2-CARBOXYLIC ACID, also known as a delta-lactam, is a chemical compound derived from piperidine-2-carboxylic acid. It is characterized by the presence of an oxo group substitution at the 6th position. This unique structure endows it with various potential applications across different industries.
Uses
Used in Pharmaceutical Industry:
6-OXO-PIPERIDINE-2-CARBOXYLIC ACID is used as an intermediate compound for the synthesis of various pharmaceutical products. Its unique structure allows it to be a key component in the development of new drugs, particularly those targeting the central nervous system.
Used in Chemical Synthesis:
In the field of organic chemistry, 6-OXO-PIPERIDINE-2-CARBOXYLIC ACID serves as a valuable building block for the creation of more complex molecules. Its delta-lactam structure makes it a versatile starting material for the synthesis of various organic compounds, including those with potential applications in materials science and specialty chemicals.
Used in Research and Development:
6-OXO-PIPERIDINE-2-CARBOXYLIC ACID is utilized as a research tool in the study of biological processes and the development of new therapeutic strategies. Its unique structure allows scientists to explore its interactions with various biological targets, potentially leading to the discovery of novel pharmacological agents.
Used in Drug Design:
6-OXO-PIPERIDINE-2-CARBOXYLIC ACID is employed as a structural element in the design of new drugs, particularly those aimed at treating neurological disorders. Its delta-lactam structure can be modified to create a variety of drug candidates with different pharmacological properties, offering a wide range of potential applications in the treatment of various diseases.
Used in Analytical Chemistry:
6-OXO-PIPERIDINE-2-CARBOXYLIC ACID can be used as a reference compound or standard in analytical chemistry. Its well-defined structure and properties make it suitable for calibrating instruments and validating analytical methods, ensuring the accuracy and reliability of experimental results.
Used in Material Science:
In the field of material science, 6-OXO-PIPERIDINE-2-CARBOXYLIC ACID may find applications as a component in the development of novel materials with specific properties. Its unique structure could be exploited to create materials with enhanced performance characteristics, such as improved mechanical strength, thermal stability, or chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 3770-22-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,7 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3770-22:
(6*3)+(5*7)+(4*7)+(3*0)+(2*2)+(1*2)=87
87 % 10 = 7
So 3770-22-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H9NO3/c8-5-3-1-2-4(7-5)6(9)10/h4H,1-3H2,(H,7,8)(H,9,10)
3770-22-7Relevant articles and documents
INHIBITORS OF HISTONE DEACETYLASE USEFUL FOR THE TREATMENT OR PREVENTION OF HIV INFECTION
-
Page/Page column 31, (2020/02/23)
The present invention relates to Compounds of Formula (I): Formula (I) and pharmaceutically acceptable salts or prodrug thereof, wherein R1, R2, R3, Ra, Rb, A and B are as defined herein. The present invention also relates to compositions comprising at least one compound of Formula (I), and methods of using the compounds of Formula (I) for treating or preventing HIV infection in a subject.
An Efficient Two-Step Preparation of α-, β-, γ- or δ-Amino Acids from 2-Pyrazinones, 2-Hydroxypyrimidines or 2-Pyridones Respectively
Zacharie, Boulos,Abbott, Shaun D.,Baigent, Christopher B.,Doyle, Christopher,Yalagala, Ravi Shekar
, p. 6486 - 6493 (2018/11/23)
A practical and efficient two-step procedure is reported for the preparation of a variety of α-, β-, γ- and δ-amino acids from 2-pyridone, 2-pyrazinone or 2-hydroxypyrimidine and derivatives. The procedure is amenable to scale-up and in most cases no chromatographic purification of the product is required. This approach is useful, especially in the synthesis of amino acids or deuterated amino acids that are not obtained by other methods.
Influence of alkylamides of glutamic acid and related compounds on the central nervous system. II. Syntheses of amides of gutamic acid and related compounds, and their effects on the central nervous system.
Kimura,Murata
, p. 1301 - 1307 (2007/10/05)
-
