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2,4-Pentadien-1-one, 1,3,5-triphenyl- is an organic compound characterized by its molecular formula C21H16O and a molar mass of 280.35 g/mol. This conjugated dienone features a pentadienone core with three phenyl groups attached at the 1, 3, and 5 positions, respectively. The compound is known for its unique electronic properties and reactivity, which arise from the interaction between the dienone system and the phenyl rings. It is often used in organic synthesis as a building block for more complex molecules, particularly in the preparation of certain pharmaceuticals and materials. The compound's structure and properties make it a subject of interest in the field of organic chemistry, where it serves as a model for studying the effects of conjugation and aromaticity on chemical behavior.

4735-00-6

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4735-00-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4735-00-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,3 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4735-00:
(6*4)+(5*7)+(4*3)+(3*5)+(2*0)+(1*0)=86
86 % 10 = 6
So 4735-00-6 is a valid CAS Registry Number.

4735-00-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-triphenylpenta-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names 1,3,5-Triphenyl-penta-2,4-dienon

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:4735-00-6 SDS

4735-00-6Downstream Products

4735-00-6Relevant academic research and scientific papers

Free radicals: XXVIII. Reaction of 2,4,6-triphenylpyranyl with (diacetoxy-λ3-iodanyl)benzene

Tanaseichuk,Pryanichnikova,Burtasov,Lisina,Dolganov

, p. 442 - 445 (2011)

The major product of the reaction of 2,4,6-triphenylpyranyl with (diacetoxy-λ3-iodanyl)benzene in acetonitrile and acetone was 2,4,6-triphenylpyrylium acetate. Analogous reaction in isopropyl alcohol resulted in the formation of methane, carbon dioxide, 1,3,5-triphenylpent-2-ene- 1,5-dione, 2-benzoyl-3,5-diphenylfuran, 1,3,5-triphenylpenta-2,4-dien-1-one, and a small amount of 2,4,6-triphenylpyrilium acetate.

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