80638-53-5 Usage
Uses
Used in Chemical Synthesis:
(sec-butylamino)(oxo)acetic acid serves as a key intermediate in the synthesis of various organic compounds due to its reactive functional groups. Its carboxylic acid and secondary amine functionalities facilitate the formation of esters, amides, and other derivatives, making it a valuable building block in organic chemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, (sec-butylamino)(oxo)acetic acid is utilized as a precursor for the development of drugs with potential therapeutic applications. Its ability to form a variety of chemical bonds allows for the creation of new molecular entities with specific biological activities.
Used in Analytical Chemistry:
(sec-butylamino)(oxo)acetic acid finds application in analytical chemistry as a reagent or a component in the development of assays and sensors. Its acidic and basic properties can be leveraged to modify the chemical environment in assays, enhancing their selectivity and sensitivity.
Used in Material Science:
In material science, (sec-butylamino)(oxo)acetic acid can be employed to modify the properties of polymers and other materials. Its functional groups can be used to introduce new functionalities or to alter the physical and chemical characteristics of materials, such as their solubility, stability, or reactivity.
Used in Environmental Applications:
(sec-butylamino)(oxo)acetic acid may also be utilized in environmental applications, such as in the treatment of wastewater or the remediation of contaminated sites. Its ability to interact with a wide range of chemicals could be harnessed to remove pollutants or to facilitate the degradation of harmful substances.
Check Digit Verification of cas no
The CAS Registry Mumber 80638-53-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,6,3 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 80638-53:
(7*8)+(6*0)+(5*6)+(4*3)+(3*8)+(2*5)+(1*3)=135
135 % 10 = 5
So 80638-53-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO3/c1-3-4(2)7-5(8)6(9)10/h4H,3H2,1-2H3,(H,7,8)(H,9,10)
80638-53-5Relevant academic research and scientific papers
Oxamic acid analogues as LDH-C4-specific competitive inhibitors
Rodriguez-Paez, Lorena,Chena-Taboada, Miguel Angel,Cabrera-Hernandez, Arturo,Cordero-Martinez, Joaquin,Wong, Carlos
experimental part, p. 579 - 586 (2012/06/01)
We performed kinetic studies to determine whether oxamate analogues are selective inhibitors of LDH-C4, owing to their potential usefulness in fertility control and treatment of some cancers. These substances were shown to be competitive inhibitors of LDH isozymes and are able to discriminate among subtle differences that differentiate the active sites of LDH-A4, LDH-B4 and LDH-C4. N-Ethyl oxamate was the most potent inhibitor showing the highest affinity for LDH-C4. However, N-propyl oxamate was the most selective inhibitor showing a high degree of selectivity towards LDH-C4. Non-polar four carbon atoms chains, linear or branched, dramatically diminished the affinity and selectivity towards LDH-C4. N-Propyl oxamate significantly reduced ATP levels, capacitation and mouse sperm motility, in line with results shown by others, suggesting that LDH-C4 plays an essential role in mouse fertility.
Synthesis, crystal structure, and insecticidal activity of novel N-alkyloxyoxalyl derivatives of 2-arylpyrrole
Zhao, Yu,Mao, Chunhui,Li, Yongqiang,Zhang, Pengxiang,Huang, Zhiqiang,Bi, Fuchun,Huang, Runqiu,Wang, Qingmin
experimental part, p. 7326 - 7332 (2010/06/11)
Two series of novel N-alkyloxyoxalyl derivatives of 2-arylpyrrole were synthesized, and their structures were characterized by 1H NMR spectroscopy, elemental analysis, and single-crystal X-ray diffraction analysis. The insecticidal activities of the new compounds were evaluated. The results of bioassays indicated that some of these title compounds exhibited excellent insecticidal activities, and their insecticidal activities against oriental armyworm, mosquito, and spider mite are comparable to those of the commercialized Chlorfenapyr.
