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1,3,5-Pentanetrione, 1-(4-chlorophenyl)-5-phenyl- is a chemical compound with the molecular formula C15H11ClO2. It is an organic compound that belongs to the class of pentanetriones, which are five-carbon ketones with three carbonyl groups. The specific structure of 1,3,5-Pentanetrione, 1-(4-chlorophenyl)-5-phenyl- features a 4-chlorophenyl group attached to the first carbon and a phenyl group attached to the fifth carbon of the pentanetrione backbone. 1,3,5-Pentanetrione, 1-(4-chlorophenyl)-5-phenyl- is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is important to note that handling and disposal of this chemical should be done with care, as it may have specific safety and environmental considerations.

1812-71-1

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1812-71-1 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

This describes the arrangement of atoms and the type of chemical bonds in the compound.

Explanation

A ketone derivative is a compound that contains a carbonyl group (C=O) and is derived from a ketone.

Explanation

The compound contains a benzene ring, which is a six-membered ring of carbon atoms with alternating single and double bonds.

Explanation

The compound has a chlorine atom attached to one of the phenyl groups.

Explanation

The compound is used as a starting material or building block in the synthesis of various chemical products.

Explanation

Due to its unique chemical structure, the compound may have potential applications in the development of new drugs and therapies.

Explanation

The compound has been investigated for its possible biological and pharmacological properties, which could be useful in the development of new drugs.

Explanation

Handling and using the compound requires caution, as it may have harmful effects on human health and the environment.

Explanation

Proper safety measures should be taken when working with 1,3,5-Pentanetrione, 1-(4-chlorophenyl)-5-phenyl- to minimize the risk of exposure and potential hazards.

Chemical structure

1,3,5-Pentanetrione, 1-(4-chlorophenyl)-5-phenyl-

Type of compound

Ketone derivative

Presence of benzene ring

Yes

Presence of chlorine atom

Yes

Applications

Synthetic intermediate in pharmaceuticals, agrochemicals, and other organic compounds

Potential applications

Medicinal chemistry

Biological and pharmacological properties

Studied for potential effects

Hazards

May pose risks to human health and the environment

Safety precautions

Exercise caution when handling and using the compound

Check Digit Verification of cas no

The CAS Registry Mumber 1812-71-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,1 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1812-71:
(6*1)+(5*8)+(4*1)+(3*2)+(2*7)+(1*1)=71
71 % 10 = 1
So 1812-71-1 is a valid CAS Registry Number.

1812-71-1Downstream Products

1812-71-1Relevant academic research and scientific papers

Thermal addition reaction of aroylketene with 1-aryl-1- trimethylsilyloxyethylenes: Aromatic substituent effects of aroylketene and aryltrimethylsilyloxyethylene on their reactivity

Saitoh,Oyama,Sakurai,Niimura,Hinata,Horiguchi,Toda,Sano

, p. 956 - 966 (2007/10/03)

The thermal addition reaction of various aroylketenes (C) generated by the thermolysis of 5-aryldioxofurans (A) to 1-aryl-1-trimethylsilyloxyethylenes gave 1,5-diarylpentane-1,3,5-triones (D) and 2,6-diaryl-4H-pyran-4-ones (E). The introduction of electron withdrawing substituents in the aroylketene and of electron donating substituents facilitated the addition reaction. The observed substituent effects and the reaction mechanism are interpreted in terms of molecular orbital analyses.

Thermal Cycloaddition of Aroylketene to 1-Aryl-1-trimethylsilyloxyethylene: A Simple Synthesis of 2,6-Diaryl-4H-pyran-4-one

Sano, Takehiro,Saitoh, Toshiaki,Toda, Jun

, p. 2139 - 2146 (2007/10/02)

Aroylketene (2) generated by pyrolytic decarbonylation of 5-aryl-2,3-dihydro-2,3-furandione (1) reacted with 1-aryl-1-trimethylsilyloxyethylene (3) in a regioselective manner to give 2,6-diaryl-4H-pyran-4-one (5) and/or 1,5-diarylpentane-1,3,5-trione (6).

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