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76234-38-3

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76234-38-3 Usage

Description

3-Pyrrolidin-1-ylpropanoic Acid HCL, also known as 3-PYRROLIDIN-1-YL-PROPIONIC ACID HCL, is an organic compound that serves as a key intermediate in the synthesis of various pharmaceuticals. It is characterized by its unique chemical structure, which includes a pyrrolidine ring and a propionic acid group. 3-PYRROLIDIN-1-YL-PROPIONIC ACID HCL plays a crucial role in the development of neuroprotective agents, particularly acylaminophenothiazines.

Uses

Used in Pharmaceutical Industry:
3-Pyrrolidin-1-ylpropanoic Acid HCL is used as a key intermediate in the synthesis of acylaminophenothiazines, which are neuroprotective agents. These agents are designed to protect the nervous system from damage and degeneration, offering potential therapeutic benefits for various neurological disorders.
In the development of acylaminophenothiazines, 3-Pyrrolidin-1-ylpropanoic Acid HCL contributes to the formation of the active pharmaceutical ingredient, which can help in managing and treating neurodegenerative conditions such as Alzheimer's disease, Parkinson's disease, and multiple sclerosis. Its role in the synthesis process highlights the importance of this compound in advancing pharmaceutical research and drug development for neurological applications.

Check Digit Verification of cas no

The CAS Registry Mumber 76234-38-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,2,3 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76234-38:
(7*7)+(6*6)+(5*2)+(4*3)+(3*4)+(2*3)+(1*8)=133
133 % 10 = 3
So 76234-38-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H13NO2/c9-7(10)3-6-8-4-1-2-5-8/h1-6H2,(H,9,10)

76234-38-3SDS

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-Pyrrolidinepropanoic acid,3-(1-Pyrrolidinyl)propionic acid

1.2 Other means of identification

Product number -
Other names 1-PYRROLIDINEPROPANOIC 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:76234-38-3 SDS

76234-38-3Relevant articles and documents

Synthesis of 3-(2-aminoethyl)-5-hydroxy-1H-pyrazole derivatives

Groselj, Uros,Kralj, David,Wagger, Jernej,Dahmann, Georg,Stanovnik, Branko,Svete, Jurij

experimental part, p. 49 - 65 (2012/03/11)

Treatment of β-keto ester 8 with hydrazines 9a-g gave 1'-substituted tert-butyl 2-(5-hydroxy-1Hpyrazol- 3-yl)ethylcarbamates 10a-e and 2-(5-oxo-2,5-dihydro-1H-pyrazol-3-yl)ethylcarbamates 11f,g. Acidolytic deprotection of 10b,c afforded the corresponding 3-(2-aminoethyl)-5-hydroxy- 1H-pyrazoles 6b,c in good yields. Acylation of 6 gave either the N-acyl compounds 12b,c and 13c, or the N,O-diacyl derivative 14. Next, three N,N-dialkyl analogues 15a,b and 26c were prepared from dimethyl acetone-1,3-dicarboxylate 21 via condensation with hydrazines 9a and 9h followed by hydrolysis of the esters 22a,b, amidation of the carboxylic acids 23a,b, and reduction of the tertiary carboxamides 24a and 25b,c. ARKAT-USA, Inc.

Synthesis, IR and NMR studies of zwitterionic ω-(1-pyrrolidine)alkanocarboxylic acids and their N-methyl derivatives

Dega-Szafran, Zofia,Przybylak, Robert

, p. 107 - 121 (2007/10/03)

Six ω-(1-pyrrolidine)alkanocarboxylic acid hydrohalides [C4H8N+H(CH2)(n)COOH · X-] and 1-(ω-carboxyalkyl)-1-methyl-pyrrolidinium hydrohalides [C4H8N+CH3(CH2)(n)COOH · X- (n = 1,2,3,4,5,10)] and their sodium and inner salts were synthesized, respectively. IR, 1H and 13C NMR spectra were analyzed with regard to the increasing distance effect on the interaction between the positive nitrogen atom with the negative carboxylic group. The configuration of the pyrrolidine ring was also discussed.

Chartreusin derivatives and salts thereof

-

, (2008/06/13)

This invention relates to a novel chartreusin derivative of the general formula (I): STR1 and a salt thereof. This chartreusin derivative and a salt thereof have an excellent antitumor activity, which is exhibited even when the site of cancer inoculation

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