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3,5-dioxo-5-phenylpentanoic acid, also known as 3,5-dioxovalerylbenzene or 3,5-dioxo-5-phenylvaleric acid, is an organic compound with the chemical formula C11H10O4. It is a white crystalline solid that is soluble in water and various organic solvents. 3,5-dioxo-5-phenylpentanoic acid is a derivative of pentanoic acid, featuring a phenyl group attached to the fifth carbon and two carbonyl groups at the third and fifth positions. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity and versatility, 3,5-dioxo-5-phenylpentanoic acid is an important building block in organic chemistry, allowing for the creation of a wide range of molecules with diverse applications.

5526-43-2

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5526-43-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5526-43-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,2 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5526-43:
(6*5)+(5*5)+(4*2)+(3*6)+(2*4)+(1*3)=92
92 % 10 = 2
So 5526-43-2 is a valid CAS Registry Number.

5526-43-2SDS

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 3,5-dioxo-5-phenylpentanoic acid

1.2 Other means of identification

Product number -
Other names 3,5-Dioxo-5-phenyl-valeriansaeure

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:5526-43-2 SDS

5526-43-2Relevant academic research and scientific papers

REACTIVITY OF 4-HYDROXY-2-PYRONES IN THE DIELS-ALDER REACTIONS

Tanyeli, Cihangir,Tarhan, Okan

, p. 2453 - 2460 (2007/10/02)

Biphenylcarboxylic acid derivatives, and some tetracyclic bridge cycloadducts have been prepared by Diels-Alder reactions of acetylenic and olefinic dienophiles with 4-hydroxy-6-phenyl-2H-pyran-2-one and its methyl ether derivative.

Novel Pyrones from Hypericum mysorense Heyne

Vishwakarma, R. A.,Kapil, R. S.,Popli, S. P.

, p. 466 - 468 (2007/10/02)

The aerial parts of Hypericum mysorense Heyne afford two new pyrones, characterised as 3-(1,1-dimethyl-2-propenyl)-6-phenyl-2,4(3H)-dioxopyran (6) and 3-(1,1-dimethyl-2-propenyl)-2-methoxy-6-phenyl-4H-pyran-4-one (8).The structures have been assigned on t

Use of β-Ketocarboxylic Acids for Syntheses of 6-Substituted 4-Hydroxy-2-pyrones and Acyclic β-Diketones

Ohta, Shunsaku,Tsujimura, Atsuhiko,Okamoto, Masao

, p. 2762 - 2768 (2007/10/02)

β-Ketocarboxylic acids including β-ketoglutaric acid half-esters were cyclized by treating them with 1,1'-carbonyl-diimidazole to give 6-substituted 3-acyl-4-hydroxy-2-pyrones in good yields. 5-Aryl-3,5-dioxo-1-pentanoic acid and monomethyl malonate gave 6-aryl-4-hydroxy-2-pyrone and dimethyl β-ketoglutarate, respectively, on similar treatment.Anibin, one of the Aniba alkaloids, was synthesized from 5-(3-pyridyl)-4-hydroxy-2-pyrone.In addition, it was confirmed that reaction of magnesium β-ketocarboxylate with acylimidazolide gave the corresponding acyclic β-diketone in excellent yield.Keywords - β-ketocarboxilic acid; biogenetic-type synthesis; 4-hydroxy-2-pyrone; β-polyketide; β-ketoglutaric acid; dehydroacetic acid; anibin; Aniba alkaloid; 3-acyl-4-hydroxy-2-pyrone; β-diketone.

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