939760-33-5 Usage
Uses
Used in Organic Synthesis:
Tert-butyl 3-(benzylamino)azetidine-1-carboxylate is employed as a key intermediate in organic synthesis for its ability to facilitate the construction of complex molecular architectures. Its presence in reactions can lead to the formation of a variety of biologically active compounds, making it a valuable component in the synthesis process.
Used in Pharmaceutical Research:
In the pharmaceutical industry, tert-butyl 3-(benzylamino)azetidine-1-carboxylate is used as a building block for the synthesis of pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications. tert-butyl 3-(benzylamino)azetidine-1-carboxylate's versatility in chemical reactions enables the exploration of novel drug candidates with improved efficacy and selectivity.
Used in Agrochemical Development:
Tert-butyl 3-(benzylamino)azetidine-1-carboxylate also finds application in the agrochemical sector, where it serves as a precursor for the synthesis of agrochemicals. Its reactivity and structural features are harnessed to create compounds that can address various agricultural needs, such as pest control and crop protection.
Overall, the utility of tert-butyl 3-(benzylamino)azetidine-1-carboxylate across different industries is a testament to its importance as a versatile chemical intermediate, with potential applications ranging from drug discovery to the development of agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 939760-33-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,9,7,6 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 939760-33:
(8*9)+(7*3)+(6*9)+(5*7)+(4*6)+(3*0)+(2*3)+(1*3)=215
215 % 10 = 5
So 939760-33-5 is a valid CAS Registry Number.
939760-33-5Relevant academic research and scientific papers
Methods of using pyruvate kinase activators
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Page/Page column 71; 72, (2016/08/23)
Described herein are methods for using compounds that activate pyruvate kinase.
Exploration of 3-aminoazetidines as triple reuptake inhibitors by bioisosteric modification of 3-α-Oxyazetidine
Han, Minsoo,Song, Chiman,Jeong, Nakcheol,Hahn, Hoh-Gyu
, p. 999 - 1004 (2014/12/11)
For a development of broad spectrum antidepressant 3-aminoazetidine derivatives, two series of compounds were explored by bioisosteric modification of 3-α-oxyazetidine. We synthesized 166 novel 3-aminoazetidine derivatives in series A and B, starting from Boc-protected 3-azetidinone (3) and Boc-protected 3-azetidinal (9) respectively, through parallel syntheses. The inhibitory reuptake activities against serotonin (5-HT), norepinephrine (NE), and dopamine (DA) neurotransmitters were measured by the Neurotransmitter Transporter Uptake Assay Kit using the human embryonic kidney 293 (HEK293) cells stably transfected with the respective three kinds of human transporters (hSERT, hNET, and hDAT). Our study aimed to identify compounds having relative inhibitory activities against hSERT > hNET > hDAT. Lead optimization including microsomal stability, CYP, hERG assay, Ames test, BBB, and PK study resulted in the identification of compound 10dl as a candidate for further studies.
NOVEL N- (4- (AZETIDINE - 1 - CARBONYL) PHENYL) - (HETERO - ) ARYLSULFONAMIDE DERIVATIVES AS PYRUVATE KINASE M2 (PMK2) MODULATORS
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Page/Page column 42-43, (2012/06/30)
Compounds of general Formula (I), and compositions comprising compounds of general formula I that modulate pyruvate kinase M2 (PKM2) are described herein. Also described herein are methods of using the compounds that modulate PKM2 in the treatment of canc
