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5211-23-4

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5211-23-4 Usage

General Description

N-Carbobenzyloxy-L-proline methyl ester is a chemical compound that is commonly used in organic synthesis and pharmaceutical research. It is a derivative of the amino acid proline and is often utilized as a substrate for the synthesis of peptides and other organic molecules. N-CARBOBENZYLOXY-L-PROLINE METHYL ESTER is known for its ability to act as a versatile building block in the creation of complex organic compounds, especially in the field of peptide chemistry. Its ester form allows for easy manipulation and modification of its molecular structure, making it a valuable tool for the development of new drugs and therapeutic agents. Overall, N-Carbobenzyloxy-L-proline methyl ester plays a crucial role in organic synthesis and drug discovery by providing a versatile and adaptable platform for the creation of various bioactive molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 5211-23-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,1 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5211-23:
(6*5)+(5*2)+(4*1)+(3*1)+(2*2)+(1*3)=54
54 % 10 = 4
So 5211-23-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H17NO4/c1-18-13(16)12-8-5-9-15(12)14(17)19-10-11-6-3-2-4-7-11/h2-4,6-7,12H,5,8-10H2,1H3/t12-/m0/s1

5211-23-4 Well-known Company Product Price

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  • Aldrich

  • (362913)  N-Z-L-prolinemethylester  97%

  • 5211-23-4

  • 362913-25G

  • 2,061.54CNY

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5211-23-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-O-benzyl 2-O-methyl (2S)-pyrrolidine-1,2-dicarboxylate

1.2 Other means of identification

Product number -
Other names N-Z-L-proline 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:5211-23-4 SDS

5211-23-4Relevant articles and documents

An efficient, stereocontrolled and versatile synthetic route to bicyclic partially saturated privileged scaffolds

Bond, Andrew D.,Hanby, Abigail R.,King, Thomas A.,Moss, Thomas A.,Sore, Hannah F.,Spring, David R.,Stewart, Hannah L.

supporting information, p. 6818 - 6821 (2020/07/04)

Herein, we describe the development of a simple, high yielding and stereocontrolled strategy for the synthesis of a series of triazolopiperazines and other biologically relevant fused scaffolds from optically active amino acids. This route was applied to the synthesis of 22 scaffolds containing new, previously inaccessible vectors and used to access a novel analogue of ganaplacide.

IDO INHIBITORS

-

Paragraph 1621, (2016/10/27)

There are disclosed compounds that modulate or inhibit the enzymatic activity of indoleamine 2,3-dioxygenase (IDO), pharmaceutical compositions containing said compounds and methods of treating proliferative disorders, such as cancer, viral infections and/or inflammatory disorders utilizing the compounds of the invention.

A lanthanide(III) triflate mediated macrolactonization/solid-phase synthesis approach for depsipeptide synthesis

Goodreid, Jordan D.,Dos Santos Da Silveira, Eduardo,Batey, Robert A.

supporting information, p. 2182 - 2185 (2015/05/13)

The effect of dysprosium(III) triflate on macrolactonization reactions to form depsipeptides using MNBA (Shiina's reagent) is reported. Improved yields were obtained for the formation of 16-membered depsipeptides using lanthanide triflate additives. The use of a macrocyclization strategy permits the use of a semiautomated solid-phase synthesis approach for the rapid synthesis of analogues of the antibacterial A54556 acyldepsipeptides in only two physical operations, requiring only final product purification after cyclization.

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