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114150-57-1

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114150-57-1 Usage

General Description

4,6-Dioxo-6-phenylhexanoic acid is a chemical compound with the molecular formula C12H10O4. It is a diketone derivative of adipic acid and contains two carbonyl groups adjacent to each other. The compound is a white crystalline solid that is sparingly soluble in water and soluble in organic solvents. 4,6-Dioxo-6-phenylhexanoic acid is used in the synthesis of pharmaceuticals and agrochemicals and as an intermediate in organic synthesis. It is also used in the production of polymers and coatings. The compound may have potential applications in the field of medicinal chemistry and drug development due to its unique structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 114150-57-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,1,5 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 114150-57:
(8*1)+(7*1)+(6*4)+(5*1)+(4*5)+(3*0)+(2*5)+(1*7)=81
81 % 10 = 1
So 114150-57-1 is a valid CAS Registry Number.

114150-57-1SDS

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 4,6-Dioxo-6-phenylhexanoic acid

1.2 Other means of identification

Product number -
Other names 4,6-dioxo-6-phenyl-hexanoic 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:114150-57-1 SDS

114150-57-1Relevant articles and documents

Synthesis of 1,5-diarylpyrazol-3-propanoic acids towards inhibition of cyclooxygenase-1/2 activity and 5-lipoxygenase-mediated LTB4 formation

Erguen, Burcu Caliskan,Nunez, Maria Teresa,Labeaga, Luis,Ledo, Francisco,Darlington, Janice,Bain, Gretchen,Cakir, Bilge,Banoglu, Erden

scheme or table, p. 497 - 505 (2011/05/09)

A set of 25 derivatives of 3-[1-(6-substituted-pyridazin-3-yl)-5-(4- substitutedphenyl)-1H-pyrazol-3-yl]propanoic acids has been synthesized and evaluated for their in vitro cyclooxygenase-1/2 (COX-1/ 2) inhibitory activity using assays with purified COX-1 and COX-2 enzymes as well as for their 5-lipoxygenase (5-LO)-mediated LTB4 formation inhibitory activity using an assay with activated human polymorphonuclear leukocytes (PMNL). Among the synthesized compounds, especially 4g showed COX-1 (IC50 = 1.5 μM) and COX-2 (IC50 = 1.6 μM) inhibitory activity, whereas compounds 4b and 4 f resulted in the inhibition of 5-LO-mediated LTB4 formation at 14 μM and 12 μM IC50 values, respectively, without any significant inhibition on COX isoforms. ECV · Editio Cantor Verlag.

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