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(2R)-2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)pentanedioic acid, also known as L-Phenylalanine Diketopiperazine, is a cyclic dipeptide derived from the amino acid phenylalanine. It is formed through the condensation of two molecules of phenylalanine, resulting in a unique structure with potential health benefits and applications.

22911-88-2

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22911-88-2 Usage

Uses

Used in Food Industry:
(2R)-2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)pentanedioic acid is used as a flavoring agent in the food industry, enhancing the taste and aroma of various products. Its natural occurrence in milk and dairy products contributes to the rich flavor profile of these items.
Used in Pharmaceutical Applications:
(2R)-2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)pentanedioic acid is being investigated for its potential pharmaceutical applications due to its antioxidant and antimicrobial properties. These characteristics make it a promising candidate for the development of new drugs and treatments.
Used in Antioxidant Applications:
As an antioxidant, (2R)-2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)pentanedioic acid can help protect cells from damage caused by free radicals and oxidative stress. This property is valuable in the development of health supplements and pharmaceuticals aimed at promoting overall well-being and preventing age-related diseases.
Used in Antimicrobial Applications:
(2R)-2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)pentanedioic acid's antimicrobial properties make it a potential candidate for use in the development of new antibiotics or as a natural preservative in various products, including food and cosmetics, to inhibit the growth of harmful microorganisms.

Check Digit Verification of cas no

The CAS Registry Mumber 22911-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,1 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 22911-88:
(7*2)+(6*2)+(5*9)+(4*1)+(3*1)+(2*8)+(1*8)=102
102 % 10 = 2
So 22911-88-2 is a valid CAS Registry Number.

22911-88-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-2-phthalimidoglutaric acid

1.2 Other means of identification

Product number -
Other names N-phthaloyl-(R)-glutamic acid

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:22911-88-2 SDS

22911-88-2Relevant academic research and scientific papers

Poly-γ-p-Biphenylmethyl-Glutamate as Enantiodifferentiating Alignment Medium for NMR Spectroscopy with Temperature-Tunable Properties

Jeziorowski, Sharon,Thiele, Christina M.

supporting information, p. 15631 - 15637 (2018/09/27)

The use of anisotropic NMR parameters—especially residual dipolar couplings (RDCs)—offers access to additional structural information and, therefore, alignment media required for this approach are under a continuous development. Here, we present poly-γ-p-biphenylmethyl-glutamate (PBPMG) as a new versatile enantiodifferentiating alignment medium. The thermoresponsive properties of this polymer allowed for RDC measurements of more than one orientation within the same sample at different temperatures. Moreover, the outstanding enantiodifferentiation along with excellent spectral quality even offered the opportunity to differentiate enantiomers in mixtures.

Palladium-catalysed asymmetric allylic substitution: Synthesis of α- and β-amino acids

Bower, Justin F.,Jumnah, Roshan,Williams, Andrew C.,Williams, Jonathan M. J.

, p. 1411 - 1420 (2007/10/03)

Methodology has been established for the formation of enantiomerically enriched α-amino acids using palladium-catalysed allylic amination. The formation of enantiomerically enriched allylamines has been achieved with high enantioselectivity. Oxidative cleavage of the allylamines provides arylglycine and glutamic acid derivatives. Additionally, enantiomerically enriched β-amino acids have been prepared in high enantiomeric excess. Palladium-catalysed asymmetric allylic substitution is used as the key synthetic transformation.

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