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(S)-3-BroMo-pyrrolidine-1-carboxylic acid benzyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1353995-89-7

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1353995-89-7 Usage

Uses

Used in Pharmaceutical Industry:
(S)-3-Bromo-pyrrolidine-1-carboxylic acid benzyl ester is used as a building block for the synthesis of various pharmaceutical compounds. Its role in creating new therapeutic agents and drug targets contributes to the development of novel treatments for a range of medical conditions.
Used in Organic Chemistry Research:
In the field of organic chemistry, (S)-3-Bromo-pyrrolidine-1-carboxylic acid benzyl ester is used as a versatile compound for conducting research and experiments. Its reactive benzyl ester group allows for further chemical modifications, making it a valuable tool for exploring new reactions and synthesizing complex organic molecules.
Used in Drug Discovery:
(S)-3-Bromo-pyrrolidine-1-carboxylic acid benzyl ester is employed as a key component in drug discovery processes. Its potential use in the development of therapeutic agents and drug targets aids researchers in identifying and creating new drugs with improved efficacy and safety profiles.

Check Digit Verification of cas no

The CAS Registry Mumber 1353995-89-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,3,9,9 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1353995-89:
(9*1)+(8*3)+(7*5)+(6*3)+(5*9)+(4*9)+(3*5)+(2*8)+(1*9)=207
207 % 10 = 7
So 1353995-89-7 is a valid CAS Registry Number.

1353995-89-7Downstream Products

1353995-89-7Relevant academic research and scientific papers

Synthesis of (+/-) - oxohexahydrofuro[3,2-b]pyrroles (pyrrolidine-trans-lactones) using acyl-iminium chemistry

Macdonald, Simon J.F.,Spooner, Julie E.,Dowle, Michael D.

, p. 1375 - 1377 (1998)

In a new synthesis of pyrrolidine-trans-lactones, an acyliminium pyrrolidine reacts with silyl ketene acetals. This reaction selectively generates C2, C3 trans stereochemistry.

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