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4,5-dihydro-3-methyl-5-oxo-1H-pyrazole-1-acetic acid is a heterocyclic carboxylic acid derivative of pyrazole with the molecular formula C6H8N2O3. It is a chemical compound of interest in medicinal chemistry and drug development research due to its potential biological and pharmaceutical relevance.

30979-39-6

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30979-39-6 Usage

Uses

Used in Pharmaceutical Industry:
4,5-dihydro-3-methyl-5-oxo-1H-pyrazole-1-acetic acid is used as a potential anti-inflammatory and analgesic agent for its potential to alleviate inflammation and pain.
Used in Medicinal Chemistry Research:
4,5-dihydro-3-methyl-5-oxo-1H-pyrazole-1-acetic acid is used as a building block for the synthesis of new pharmaceutical compounds, leveraging its structure and reactivity to create novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 30979-39-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,9,7 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 30979-39:
(7*3)+(6*0)+(5*9)+(4*7)+(3*9)+(2*3)+(1*9)=136
136 % 10 = 6
So 30979-39-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H8N2O3/c1-4-2-5(9)8(7-4)3-6(10)11/h2-3H2,1H3,(H,10,11)

30979-39-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-methyl-5-oxo-4H-pyrazol-1-yl)acetic acid

1.2 Other means of identification

Product number -
Other names 4,5-Dihydro-3-methyl-5-oxo-1H-pyrazole-1-acetic 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:30979-39-6 SDS

30979-39-6Downstream Products

30979-39-6Relevant academic research and scientific papers

Site-Specific Tandem Knoevenagel Condensation-Michael Addition to Generate Antibody-Drug Conjugates

Kudirka, Romas A.,Barfield, Robyn M.,McFarland, Jesse M.,Drake, Penelope M.,Carlson, Adam,Banas, Stefanie,Zmolek, Wes,Garofalo, Albert W.,Rabuka, David

, p. 994 - 998 (2016)

Expanded ligation techniques are sorely needed to generate unique linkages for the growing field of functionally enhanced proteins. To address this need, we present a unique chemical ligation that involves the double addition of a pyrazolone moiety with an aldehyde-labeled protein. This ligation occurs via a tandem Knoevenagel condensation-Michael addition. A pyrazolone reacts with an aldehyde to generate an enone, which undergoes subsequent attack by a second pyrazolone to generate a bis-pyrazolone species. This rapid and facile ligation technique is performed under mild conditions in the absence of catalyst to generate new architectures that were previously inaccessible via conventional ligation reactions. Using this unique ligation, we generated three site-specifically labeled antibody-drug conjugates (ADCs) with an average of four drugs to one antibody. The in vitro and in vivo efficacies along with pharmacokinetic data of the site-specific ADCs are reported.

Pyrazolone-based glycoprotein-bound membrane dye as well as preparation method and application thereof

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Paragraph 0067; 0075-0078, (2021/08/07)

The invention discloses a pyrazolone-based glycoprotein-bound membrane dye. The general formula structure of the membrane dye is as shown in formula (I), and in the formula (I), R1 is a fluorescent chromophore dye structure with an O terminal or an N terminal; R2 is at least one selected from -O-, -O-O-, -S-, -NH-, -NHNH- or -ONH-; and R3 is at least one selected from the shown groups. The invention relates to a biosensor for long-retention cell membrane tracking imaging, and/or for rapid and accurate imaging of cell membranes at low concentrations, and/or for observing cell division and migration processes, and/or for membrane labeling to distinguish co-cultured cells, and/or for distinguishing fluorescence signals of different cells, and/or for labeling and grouping of cells, and/or for tracking of passage cells.

Thrombopoietin mimetics

-

, (2008/06/13)

Invented are non-peptide TPO mimetics. Also invented is a method of treating thrombocytopenia, in a mammal, including a human, in need thereof which comprises administering to such mammal an effective amount of a selected azo-pyrazole derivative.

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