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2,4-DIMETHYL-3-PYRROLEPROPIONIC ACID, a carboxylic acid derivative of pyrrole with the molecular formula C9H11NO2, is a chemical compound that serves as a versatile intermediate in the synthesis of pharmaceuticals and agrochemicals. It has garnered interest for its potential pharmacological properties, such as anti-inflammatory and analgesic effects, as well as its role in the treatment of neurological disorders and as a neuroprotective agent.

54474-50-9

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54474-50-9 Usage

Uses

Used in Pharmaceutical Industry:
2,4-DIMETHYL-3-PYRROLEPROPIONIC ACID is used as a key intermediate in the synthesis of various pharmaceuticals for its potential to contribute to the development of drugs with anti-inflammatory and analgesic properties. Its role in the synthesis process is crucial for creating medications that can alleviate pain and reduce inflammation.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4-DIMETHYL-3-PYRROLEPROPIONIC ACID is utilized as an intermediate in the production of agrochemicals, highlighting its versatility and importance in different chemical applications.
Used in Neurological Disorder Treatment:
2,4-DIMETHYL-3-PYRROLEPROPIONIC ACID is studied for its potential role in treating neurological disorders, given its pharmacological properties that may help in managing the symptoms and progression of such conditions.
Used as a Neuroprotective Agent:
2,4-DIMETHYL-3-PYRROLEPROPIONIC ACID is also being investigated for its neuroprotective capabilities, suggesting that it could be instrumental in safeguarding the nervous system from damage or degeneration, thereby offering therapeutic benefits in neurodegenerative diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 54474-50-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,4,7 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54474-50:
(7*5)+(6*4)+(5*4)+(4*7)+(3*4)+(2*5)+(1*0)=129
129 % 10 = 9
So 54474-50-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NO2/c1-6-5-10-7(2)8(6)3-4-9(11)12/h5,10H,3-4H2,1-2H3,(H,11,12)

54474-50-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2,4-dimethyl-1H-pyrrol-3-yl)propanoic acid

1.2 Other means of identification

Product number -
Other names 2,4-Dimethyl-3-Pyrrolepropionic 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:54474-50-9 SDS

54474-50-9Relevant academic research and scientific papers

Boradiazaindacene dyes for technology of biological microchips

Belobritskaya,Neunylova,Vasiliskov,Rumyantseva,Chudinov,Zasedatelev

, p. 617 - 619 (2007)

A number of boradiazaindacene dyes containing a carboxyl group separated from a fluorophore by two methylene units were synthesized. The compounds have narrow spectral bands with absorption maxima at 480-530 nm and fluorescence maxima at 500-550 nm. Succinimide esters of these compounds and the corresponding fluorescent-labeled oligonucleotides were also prepared. Boradiazaindacene dyes can be used as fluorescent labels for oligonucleotides for analysis of melting curves of duplexes on microchips either by themselves or in combination with Texas Red. They can also be applied for labeling primers for polymerase chain reaction.

5-sulfonamido-substituted indolinone compounds as protein kinase inhibitors

-

Page/Page column 16-17, (2010/02/08)

The present invention relates to 5-sulfonamido substituted indolinones that modulate the activity of protein kinases (“PKs”). The compounds of this invention are therefore useful in treating disorders related to abnormal PK activity. Pharmaceutical compositions comprising these compounds, methods of treating diseases utilizing pharmaceutical compositions comprising these compounds and methods of preparing them are also disclosed.

Sulfonamide substituted indolinones as inhibitors of DNA dependent protein kinase (DNA-PK)

-

Page 12, (2010/02/10)

The present invention relates generally to the field of radiosensitizing agents which are capable of enhancing radiotherapy by inhibiting DNA-PK (DNA-protein kinase). In particular, it relates to sulfonamide substituted indolinones which inhibit DNA-PK.

Pyrrole substituted 2-indolinone protein kinase inhibitors

-

, (2008/06/13)

The present invention relates to novel pyrrole substituted 2-indolinone compounds and physiologically acceptable salts and prodrugs thereof which modulate the activity of protein kinases and therefore are expected to be useful in the prevention and treatment of protein kinase related cellular disorders such as cancer.

Bromination of Dipyrromethenes for Porphyrin Synthesis

Paine, John B.,Hiom, John,Dolphin, David

, p. 2796 - 2802 (2007/10/02)

5'-Bromo-5-(bromomethyl)-2,2'-dipyrromethenium bromides (1) and dimers were prepared in 90percent yield from 5'-unsubstituted (16), 5'-carboxy- (15),or 5'-bromo-5-methyl-2,2'-dipyrromethenium bromides (17) by treatment of the latter with bromine and trifluoroacetic acid in chlorocarbon solvents at room temperature.Dipyrromethenes (1) are important intermediates in the Johnson regioselective synthesis of porphyrins via biladienes (3).Improvements in porphyrin synthetic methodology are exemplified by the preparation of etioporphyrin III (4a) and mesoporphyrin II dimethyl ester (4b)

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