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PYRROLIDIN-1-YL-ACETIC ACID, also known as 1-Pyrrolidineacetic Acid, is an organic compound with the chemical structure featuring a pyrrolidine ring and an acetic acid group. It is a versatile molecule that serves as a key intermediate in the synthesis of various pharmaceuticals and other chemical products. Its unique structure allows it to participate in a wide range of organic reactions, making it a valuable compound in the field of chemistry.

37386-15-5

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37386-15-5 Usage

Uses

Used in Pharmaceutical Industry:
PYRROLIDIN-1-YL-ACETIC ACID is used as a reactant and reagent for the synthesis of various pharmaceutical compounds. Its ability to participate in different organic reactions makes it a crucial component in the development of new drugs and medications.
Used in Cosmetic Industry:
PYRROLIDIN-1-YL-ACETIC ACID is used as an active ingredient in cosmetic products, particularly those aimed at preventing or ameliorating wrinkles. Its incorporation into these products helps to improve skin elasticity and reduce the appearance of fine lines and wrinkles, providing anti-aging benefits to users.

Check Digit Verification of cas no

The CAS Registry Mumber 37386-15-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,3,8 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 37386-15:
(7*3)+(6*7)+(5*3)+(4*8)+(3*6)+(2*1)+(1*5)=135
135 % 10 = 5
So 37386-15-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO2/c8-6(9)5-7-3-1-2-4-7/h1-5H2,(H,8,9)

37386-15-5SDS

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 2-(Pyrrolidin-1-yl)acetic acid

1.2 Other means of identification

Product number -
Other names Pyrrolidin-1-ylacetic 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:37386-15-5 SDS

37386-15-5Relevant academic research and scientific papers

Nitrogen-containing cyclic compounds as iminium ion sources for selected reaction monitoring detection of derivatized analytes

?ilionis, Andrius

supporting information, p. 25 - 35 (2019/09/03)

Liquid chromatography–tandem mass spectrometry is one of the most sensitive tools for determination of trace amounts of analytes in metabolomics and proteomics. The highest sensitivity is achieved in selected reaction monitoring detection, which involves fragmentation of the molecular ion between two levels of mass selection. However, fragmentation of some compounds is complicated. Detection sensitivity of such analytes may be increased by derivatizing them with a specific moiety fragmentation of which results in product ion of high abundance. In this work, we reveal the influence of iminium ions' structures on their stability by comparing six nitrogen-containing cyclic compounds as derivatization reagents for tandem mass spectrometric analysis of amino group-containing analyte. Commercially available starting materials (piperidine, 2,6-dimethylpiperidine, 1-methylpiperazine, morpholine, pyrrolidine and 1-cyanomethyl-3-methylimidazolium ionic liquid) were used for the synthesis of corresponding carboxylic acids which were further used for derivatization of the model analyte tryptamine. Liquid chromatographic–mass spectrometric analysis of differently derivatized tryptamine was performed for the evaluation of release and stability of corresponding iminium ions under collision-induced dissociation conditions. As a result, morpholine moiety was shown being the most promising iminium ion source among tested compounds. Possible sub-fragmentation pathways of investigated iminium ions were discussed, and the structures of secondary product ions were proposed.

Reagent-free continuous thermal tert-butyl ester deprotection

Cole, Kevin P.,Ryan, Sarah J.,Groh, Jennifer McClary,Miller, Richard D.

, p. 6209 - 6217 (2017/09/30)

Continuous processing enables the use of non-standard reaction conditions such as high temperatures and pressures while in the liquid phase. This expands the chemist's toolbox and can enable previously unthinkable chemistry to proceed with ease. For a series of amphoteric amino acid derivatives, we have demonstrated the ability to hydrolyze the tert-butyl ester functionality in protic solvent systems. Using a continuous plug flow reactor at 120–240 °C and 15–40 min reaction times, no pH modification or additional reagents are needed to achieve the desired transformation. The method was then expanded to encompass a variety of more challenging substrates to test selectivity and racemization potential. The acid products were generally isolated as crystalline solids by simple solvent exchange after the deprotection reaction in good to high yield and purity.

PROTEIN KINASE INHIBITORS

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Paragraph 0161, (2015/02/18)

A compound of formula (I), wherein R3, R4, G, B, M, and Z are as defined in the claims, and pharmaceutically acceptable salts thereof are disclosed. The compounds of formula (I) possess utility as FGFR inhibitors and are useful in the treatment of a condition, where FGFR kinase inhibition is desired, such as cancer.

PROTEIN KINASE INHIBITORS

-

Page/Page column 40, (2013/04/25)

A compound of formula (I), wherein R3, R4, G, B, M, and Z are as defined in the claims, and pharmaceutically acceptable salts thereof are disclosed. The compounds of formula (I) possess utility as FGFR inhibitors and are useful in the treatment of a condition, where FGFR kinase inhibition is desired, such as cancer.

TIGECYCLINE AND METHODS OF PREPARATION

-

Page/Page column 61, (2010/11/25)

Methods of preparing and purifying tetracyclines, such as tigecycline, are disclosed. Also disclosed are tetracycline compositions, such as tigecycline compositions, prepared by these methods.

METHODS OF PURIFYING TIGECYCLINE

-

Page/Page column 61, (2010/11/25)

Methods of preparing and purifying tetracyclines, such as tigecycline, are disclosed. Also disclosed are tetracycline compositions, such as tigecycline compositions, prepared by these methods.

TIGECYCLINE AND METHODS OF PREPARING 9-AMINOMINOCYCLINE

-

Page/Page column 60-61, (2010/11/25)

Methods of preparing and purifying tetracyclines, such as tigecycline, are disclosed. Also disclosed are tetracycline compositions, such as tigecycline compositions, prepared by these methods.

TIGECYCLINE AND METHODS OF PREPARING 9-NITROMINOCYCLINE

-

Page/Page column 62, (2010/11/25)

Methods of preparing and purifying tetracyclines, such as tigecycline, are disclosed. Also disclosed are tetracycline compositions, such as tigecycline compositions, prepared by these methods.

NK1 and NK3 antagonists

-

Page/Page column 27, (2010/02/14)

The invention is to a compound exhibiting neurokinin inhibitory properties, a pharmaceutical composition comprising same and a method of treatment for neurokinin-mediated conditions.

Synthesis and pharmacological evaluation of glycine-modified analogues of the neuroprotective agent glycyl-L-prolyl-L-glutamic acid (GPE)

Lai, Michelle Y.H.,Brimble, Margaret A.,Callis, David J.,Harris, Paul W.R.,Levi, Mark S.,Sieg, Frank

, p. 533 - 548 (2007/10/03)

The synthesis of 10 G*PE analogues, wherein the glycine residue has been modified, is described by coupling readily accessible dibenzyl-l-prolyl-l- glutamate 2 with various analogues of glycine. Pharmacological evaluation of the novel compounds was undertaken to further understand the role of the glycine residue on the observed neuroprotective properties of the endogenous tripeptide GPE.

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