160233-42-1 Usage
Description
METHYL (R)-1-TRITYL-2-AZIRIDINECARBOXYLATE, a chemical compound with the formula C23H21NO3, is a derivative of aziridine. It features a trityl-protected aziridine ring and a methyl ester functional group, making it a versatile reagent in organic synthesis. METHYL (R)-1-TRITYL-2-AZIRIDINECARBOXYLATE is recognized for its potential biological activity and is considered a promising building block in the pharmaceutical and chemical industries for the synthesis of a variety of organic compounds.
Uses
Used in Pharmaceutical Industry:
METHYL (R)-1-TRITYL-2-AZIRIDINECARBOXYLATE is used as a pharmaceutical intermediate for its potential biological activity. It serves as a key component in the development of new drugs, leveraging its unique structure to contribute to medicinal chemistry advancements.
Used in Chemical Industry:
In the chemical industry, METHYL (R)-1-TRITYL-2-AZIRIDINECARBOXYLATE is used as a building block in organic synthesis. Its trityl-protected aziridine ring and methyl ester functional group make it a valuable precursor for creating a range of organic compounds, enhancing the diversity of chemical products available for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 160233-42-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,2,3 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 160233-42:
(8*1)+(7*6)+(6*0)+(5*2)+(4*3)+(3*3)+(2*4)+(1*2)=91
91 % 10 = 1
So 160233-42-1 is a valid CAS Registry Number.
InChI:InChI=1/C23H21NO2/c1-26-22(25)21-17-24(21)23(18-11-5-2-6-12-18,19-13-7-3-8-14-19)20-15-9-4-10-16-20/h2-16,21H,17H2,1H3/t21-,24?/m1/s1
160233-42-1Relevant articles and documents
Method for catalyzing asymmetric Henry reaction of trifluoromethyl ketone
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Paragraph 0192; 0195-0196, (2021/03/06)
The invention provides a method for catalyzing asymmetric Henry reaction of trifluoromethyl ketone. The method adopts a brand-new catalyst namely a compound shown as a formula I, and is simple to operate, high in substrate universality, high in reaction y
Total synthesis and activity of the metallo-β-lactamase inhibitor aspergillomarasmine A
Koteva, Kalinka,King, Andrew M.,Capretta, Alfredo,Wright, Gerard D.
supporting information, p. 2210 - 2212 (2016/02/19)
Resistance to β-lactam antibiotics is mediated primarily by enzymes that hydrolytically inactivate the drugs by one of two mechanisms: serine nucleophilic attack or metal-dependent activation of a water molecule. Serine β-lactamases are countered in the c
Studies on the synthesis of orthogonally protected azalanthionines, and of routes towards β-methyl azalanthionines, by ring opening of N-activated aziridine-2-carboxylates
O'Brien, Keith,ó Proinsias, Keith,Kelleher, Fintan
, p. 5082 - 5092 (2014/07/08)
Orthogonally protected azalanthionines were successfully synthesised by the ring-opening of N-activated aziridine-2-carboxylates with protected diaminopropanoic acids (DAPs). The required DAPs were also prepared by ring-opening of N-activated aziridine-2-carboxylates with para- methoxybenzylamine, but it was found that the choice of aziridine protecting groups dictated both the success of the reaction as well as the regioselectivity of the isolated products. Attempts to extend the methodology to the preparation of the more sterically demanding β-methyl azalanthionines have, so far, been unsuccessful.