67809-62-5 Usage
Uses
Used in Pharmaceutical Synthesis:
AMINO-(3,5-DIMETHYL-1H-PYRAZOL-4-YL)-ACETIC ACID is used as a building block for the development of pharmaceuticals due to its versatile chemical structure and potential biological activity.
Used in Medicinal Chemistry:
It is employed as a key component in the design and synthesis of new drugs, leveraging its anti-inflammatory and analgesic properties for therapeutic applications.
Used in Organic Synthesis:
AMINO-(3,5-DIMETHYL-1H-PYRAZOL-4-YL)-ACETIC ACID is used as a precursor in the synthesis of various organic compounds, contributing to the development of new materials and chemical processes.
Used in Therapeutics:
It is utilized as a therapeutic agent for its potential role in treating conditions that may benefit from its anti-inflammatory and analgesic effects, although further research is required to fully understand its clinical applications.
Used in Research and Development:
AMINO-(3,5-DIMETHYL-1H-PYRAZOL-4-YL)-ACETIC ACID is used in research settings to explore its potential in the development of new materials and to understand its biological activity for future applications in medicine and other industries.
Check Digit Verification of cas no
The CAS Registry Mumber 67809-62-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,8,0 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 67809-62:
(7*6)+(6*7)+(5*8)+(4*0)+(3*9)+(2*6)+(1*2)=165
165 % 10 = 5
So 67809-62-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H11N3O2/c1-3-5(4(2)10-9-3)6(8)7(11)12/h6H,8H2,1-2H3,(H,9,10)(H,11,12)
67809-62-5Relevant academic research and scientific papers
Synthesis and spectroscopy of novel-α-pyrazolylglycine derivatives
Zia-ul-Haq, Muhammad,Arshad, Muhammad,Saeed-ur-Rehman
, p. 45 - 48 (2007/10/03)
The synthesis of α-pyrazolylglycine derivatives (7a-d) with different substituents, starting from glycine have been prepared. The spectroscopy of intermediate compounds and the final amino acids have been discussed.
A radical-organometallic glycine synthon. Preparation of homochiral heterocyclic α-amino acids
Lloris,Moreno-Manas
, p. 7119 - 7122 (2007/10/02)
Co(Acac)2 reacts with (1) and (d)-menthyl N-BOC-2-bromoglycinates to give (1)- and (d)-menthyl N-BOC-3-acetylnorvalinates, which are converted into homochiral 2-(3,5-dimethyl-4-pyrazolyl)glycine and 2-(3,5-dimethyl)-4-isoxazolylglycine.
