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Tert-butyl 1-(phenylmethyl)-2,5-dihydropyrrole-3-carboxylate is a chemical compound that belongs to the class of organic compounds known as esters. It is derived from the combination of tert-butyl, phenylmethyl, and dihydropyrrole-3-carboxylate groups. tert-butyl 1-(phenylmethyl)-2,5-dihydropyrrole-3-carboxylate exhibits potential biological activity and may have applications in pharmaceuticals or as a building block in organic synthesis. With a molecular formula of C21H27NO2 and a molecular weight of 325.44 g/mol, it also holds promise for use in the field of medicinal chemistry or as a precursor for the synthesis of other organic compounds.

698358-08-6

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698358-08-6 Usage

Uses

Used in Pharmaceutical Industry:
Tert-butyl 1-(phenylmethyl)-2,5-dihydropyrrole-3-carboxylate is used as a pharmaceutical intermediate for its potential biological activity. It serves as a key component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Organic Synthesis:
In the field of organic synthesis, tert-butyl 1-(phenylmethyl)-2,5-dihydropyrrole-3-carboxylate is used as a building block for the synthesis of more complex organic compounds. Its unique structure allows for the creation of a variety of molecules with diverse applications.
Used as a Precursor in Synthesis:
Tert-butyl 1-(phenylmethyl)-2,5-dihydropyrrole-3-carboxylate is utilized as a precursor in the synthesis of other organic compounds, enabling the production of a wide range of chemical entities with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 698358-08-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,8,3,5 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 698358-08:
(8*6)+(7*9)+(6*8)+(5*3)+(4*5)+(3*8)+(2*0)+(1*8)=226
226 % 10 = 6
So 698358-08-6 is a valid CAS Registry Number.

698358-08-6Relevant articles and documents

A rapid catalytic asymmetric synthesis of 1,3,4-trisubstituted pyrrolidines

Belyk, Kevin M.,Beguin, Charlotte D.,Palucki, Michael,Grinberg, Nelu,DaSilva, Jimmy,Askin, David,Yasuda, Nobuyoshi

, p. 3265 - 3268 (2004)

The asymmetric synthesis of 1,3,4-trisubstituted pyrrolidines was accomplished in two steps from readily available starting materials. A 1,3-dipolar cycloaddition of an azomethine ylide to a propiolate ester followed by a Rh-catalyzed asymmetric 1,4-arylation of the resulting pyrroline with an arylboronic acid provided the desired 1,3,4-trisubstituted pyrrolidine products in good to excellent enantioselectivities.

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