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(R)-1-Benzyl-azetidine-2-carboxylic acid methyl ester is a chemical compound characterized by the molecular formula C14H17NO2. It is a methyl ester derivative of (R)-1-benzyl-azetidine-2-carboxylic acid, serving as a crucial building block for the synthesis of a variety of pharmaceutical compounds. (R)-1-Benzyl-azetidine-2-carboxylic acid methyl ester is distinguished by its unique structural and pharmacological properties, which make it a promising candidate for applications in medicinal chemistry and drug discovery.

205443-23-8

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205443-23-8 Usage

Uses

Used in Pharmaceutical Research and Development:
(R)-1-Benzyl-azetidine-2-carboxylic acid methyl ester is utilized as a key intermediate in the synthesis of various drugs and bioactive molecules. Its unique molecular structure allows for the exploration of structure-activity relationships of bioactive compounds, thereby enhancing the discovery and development of new pharmaceutical agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (R)-1-Benzyl-azetidine-2-carboxylic acid methyl ester is employed as a valuable tool for studying the interactions between chemical compounds and biological targets. Its structural features contribute to a better understanding of the mechanisms of action of potential drugs, facilitating the optimization of drug candidates for improved efficacy and safety.
Used in Drug Synthesis:
(R)-1-Benzyl-azetidine-2-carboxylic acid methyl ester is used as a starting material or intermediate in the synthesis of complex drug molecules. Its reactivity and functional groups enable the formation of diverse chemical entities, which can be further modified to achieve desired pharmacological properties.
Used in Drug Discovery:
In drug discovery, (R)-1-Benzyl-azetidine-2-carboxylic acid methyl ester serves as a versatile scaffold for the design of novel bioactive compounds. Its unique structural features can be exploited to develop new chemical entities with potential therapeutic applications, contributing to the advancement of pharmaceutical research.
Overall, (R)-1-Benzyl-azetidine-2-carboxylic acid methyl ester holds significant potential in the pharmaceutical industry, playing a vital role in the synthesis, research, and development of innovative drug candidates and bioactive molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 205443-23-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,4,4 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 205443-23:
(8*2)+(7*0)+(6*5)+(5*4)+(4*4)+(3*3)+(2*2)+(1*3)=98
98 % 10 = 8
So 205443-23-8 is a valid CAS Registry Number.

205443-23-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl (2R)-1-benzyl-2-azetidinecarboxylate

1.2 Other means of identification

Product number -
Other names N-benzylalanine methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:205443-23-8 SDS

205443-23-8Downstream Products

205443-23-8Relevant academic research and scientific papers

Highly efficient and enantioselective biotransformations of racemic azetidine-2-carbonitriles and their synthetic applications

Leng, Dong-Hui,Wang, De-Xiang,Pan, Jie,Huang, Zhi-Tang,Wang, Mei-Xiang

experimental part, p. 6077 - 6082 (2009/12/26)

(Chemical Equation Presented) Catalyzed by the Rhodococcus erythropolis AJ270 whole cell catalyst in neutral aqueous buffer at 30 °C, a number of racemic 1-benzylazetidine-2-carbonitriles, trans-1-benzyl-4-methylazetidine-2- carbonitrile, and 1-benzyl-2-m

Enzymatic resolution of methyl N-alkyl-azetidine-2-carboxylates by Candida antarctica lipase-mediated ammoniolysis

Starmans, Wim A. J.,Doppen, Roy G.,Thijs, Lambertus,Zwanenburg, Binne

, p. 429 - 435 (2007/10/03)

A facile method for the synthesis of optically active azetidine-2- carboxylic acid derivatives is presented Racemic N-alkylated azetidine esters are resolved by lipase from Candida antarctica in an ammoniolysis reaction, and both the S-amide and the R-ester are obtained with excellent stereoselectivity.

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