161596-63-0 Usage
Description
(2R,4R)-(+)-Azetidine-2,4-dicarboxylic acid is a white to off-white powdery compound with unique chemical properties. It is a chiral molecule with specific stereochemistry, which makes it valuable for various applications in the field of pharmaceuticals and biochemistry.
Uses
Used in Pharmaceutical Research:
(2R,4R)-(+)-Azetidine-2,4-dicarboxylic acid is used as a research compound for studying the function and modulation of metabotropic glutamate (mGlu) receptor subtypes. Its unique structure allows it to interact with these receptors, providing insights into their role in various physiological processes and potential therapeutic applications.
Used in Chemical Synthesis:
(2R,4R)-(+)-Azetidine-2,4-dicarboxylic acid can be used as a building block or intermediate in the synthesis of more complex molecules, particularly those with potential pharmaceutical or biological activity. Its chiral nature and functional groups make it a versatile starting material for the development of novel compounds.
Used in Analytical Chemistry:
The compound can also be employed in analytical chemistry as a reference material or standard for the development and validation of analytical methods, such as chiral chromatography or mass spectrometry, which are used to separate and identify enantiomers and other stereoisomers.
Check Digit Verification of cas no
The CAS Registry Mumber 161596-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,5,9 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 161596-63:
(8*1)+(7*6)+(6*1)+(5*5)+(4*9)+(3*6)+(2*6)+(1*3)=150
150 % 10 = 0
So 161596-63-0 is a valid CAS Registry Number.
161596-63-0Relevant articles and documents
Synthesis of optically active azetidine-2,4-dicarboxylic acid and related chiral auxiliaries for asymmetric synthesis
Hoshino, Jun'ichi,Hiraoka, Junko,Hata, Yasuo,Sawada, Seiji,Yamamoto, Yukio
, p. 693 - 698 (2007/10/02)
(S)-1-Phenylethylamine has been used as a chiral auxiliary as well as a nitrogen atom donor in the synthesis of an enantiomeric pair of azetidine-2,4-dicarboxylic acids, the absolute configuration of one of which has been assigned on the basis of the X-ra
Azetidine derivatives to treat memory and learning disorders
-
, (2008/06/13)
This invention relates to novel azetidines and derivatives thereof, as well as to pharmaceutical compositions and methods of treating memory and learning disorders. Another aspect of the invention relates to a method of utilizing the compounds and composi
Azetidine derivatives, compositions and methods of treating
-
, (2008/06/13)
This invention relates to novel azetidines and derivative thereof, as well as to pharmaceutical compositions and methods of treating memory and learning disorders. Another aspect of the invention relates to a method of utilizing the compounds and compositions as biological tools and materials for characterizing excitatory amino acid receptor systems. A further aspect of the invention relates to a method of treating PCP toxicity and abuse.
