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959573-98-9

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  • N-t-Butoxycarbonyl-trans-4-(4-iodobenzyl)-L-proline;(2S,4R)-1-t-Butoxycarbonyl-4-(4-iodobenzyl)pyrrolidine-2-carboxylic acid

    Cas No: 959573-98-9

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  • (2S,4R)-1-(tert-butoxycarbonyl)-4-(4-iodobenzyl)pyrrolidine-2-carboxylic acid

    Cas No: 959573-98-9

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959573-98-9 Usage

Description

(2S,4R)-1-(tert-Butoxycarbonyl)-4-(4-iodobenzyl)pyrrolidine-2-carboxylic acid is a chemical compound with the molecular formula C18H24INO4. It is a derivative of pyrrolidine-2-carboxylic acid, featuring a tert-butyloxycarbonyl (Boc) protecting group attached to the amine group and a 4-iodobenzyl group attached to the pyrrolidine ring. (2S,4R)-1-(tert-Butoxycarbonyl)-4-(4-iodobenzyl)pyrrolidine-2-carboxylic acid is known for its versatility in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive compounds.

Uses

Used in Pharmaceutical Synthesis:
(2S,4R)-1-(tert-Butoxycarbonyl)-4-(4-iodobenzyl)pyrrolidine-2-carboxylic acid serves as a key building block in the synthesis of various pharmaceuticals. Its unique structure allows for selective removal of the Boc protecting group under mild conditions, facilitating further molecular manipulation for the development of new drugs.
Used in Bioactive Compound Preparation:
(2S,4R)-1-(tert-Butoxycarbonyl)-4-(4-iodobenzyl)pyrrolidine-2-carboxylic acid is also utilized in the preparation of bioactive compounds, where its 4-iodobenzyl group can be employed for introducing the compound into different chemical reactions. This feature enhances its applicability in the creation of molecules with potential biological activity.
Used in Organic Synthesis:
(2S,4R)-1-(tert-Butoxycarbonyl)-4-(4-iodobenzyl)pyrrolidine-2-carboxylic acid is a versatile chemical used in a range of synthetic applications. Its ability to participate in various chemical reactions makes it a valuable component in the synthesis of complex organic molecules.
Used in Labeling Purposes:
The 4-iodobenzyl group present in the compound can also be used for labeling purposes, allowing researchers to track and study the behavior of the molecule in different chemical and biological contexts. This application is particularly useful in research and development for understanding molecular interactions and mechanisms.

Check Digit Verification of cas no

The CAS Registry Mumber 959573-98-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,9,5,7 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 959573-98:
(8*9)+(7*5)+(6*9)+(5*5)+(4*7)+(3*3)+(2*9)+(1*8)=249
249 % 10 = 9
So 959573-98-9 is a valid CAS Registry Number.

959573-98-9Upstream product

959573-98-9Downstream Products

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