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66832-97-1

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66832-97-1 Usage

Description

1-(2,4-Bis(benzoyloxy)phenyl)ethanone is an organic compound characterized by its chemical formula C28H20O5. It is a white crystalline solid known for its utility as a UV-curing agent and as a key component in the synthesis of pharmaceuticals and dyes. 1-(2,4-Bis(benzoyloxy)phenyl)ethanone features two benzoyloxy groups attached to a phenyl ring, which is connected to an ethanone group, endowing it with reactivity and versatility that make it valuable across various industries.

Uses

Used in Chemical Industry:
1-(2,4-Bis(benzoyloxy)phenyl)ethanone is used as a UV-curing agent for [application reason] its ability to facilitate the curing process of various products, enhancing their production efficiency and quality.
Used in Pharmaceutical Industry:
1-(2,4-Bis(benzoyloxy)phenyl)ethanone is used as a raw material for [application reason] its role in the synthesis of various pharmaceuticals, contributing to the development of new drugs and treatments.
Used in Dye Production:
1-(2,4-Bis(benzoyloxy)phenyl)ethanone is used as a starting material for [application reason] its involvement in the production of different types of dyes, which are essential for coloring fabrics, plastics, and other materials.
Used in Organic Synthesis:
1-(2,4-Bis(benzoyloxy)phenyl)ethanone is used as a versatile building block for [application reason] its reactivity in creating a wide range of organic compounds, which can be applied in various fields, including materials science and specialty chemicals.
Used in UV-curable Coatings and Inks:
1-(2,4-Bis(benzoyloxy)phenyl)ethanone is used as a photoinitiator for [application reason] its capacity to initiate the curing process of UV-curable coatings and inks, leading to faster drying times and improved product performance.

Check Digit Verification of cas no

The CAS Registry Mumber 66832-97-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,8,3 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 66832-97:
(7*6)+(6*6)+(5*8)+(4*3)+(3*2)+(2*9)+(1*7)=161
161 % 10 = 1
So 66832-97-1 is a valid CAS Registry Number.

66832-97-1SDS

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-acetyl-3-benzoyloxyphenyl) benzoate

1.2 Other means of identification

Product number -
Other names 2.4-Dibenzoyloxy-acetophenon

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:66832-97-1 SDS

66832-97-1Relevant articles and documents

One-pot synthesis of 3-fluoroflavones: Via 1-(2-hydroxyphenyl)-3-phenylpropane-1,3-diones and selectfluor at room temperature

Wang, Rui,Han, Jie,Li, Chenchen,Zhang, Jie,Liang, Yong,Wang, Tao,Zhang, Zunting

supporting information, p. 2479 - 2488 (2018/04/12)

A concise and efficient one-pot strategy to synthesize 3-fluoroflavones was developed. 1-(2-Hydroxyphenyl)-3-phenylpropane-1,3-diones were fluorinated using selectfluor with a small amount of CH3CN at room temperature, followed by cyclization a

Crystal structure and luminescence properties of 4-(4-benzoyloxy-2- hydroxyphenyl)-2,2-difluoro-6-phenyl-1,3,2-dioxaborine

Bukvetskii,Fedorenko,Mirochnik

, p. 1991 - 1998 (2014/07/07)

The crystal structure of 4-(4-benzoyloxy-2-hydroxyphenyl)-2,2- difluoro6phenyl-1,3,2-dioxaborine (1) was determined by X-ray diffraction analysis. π-π-Stacking interaction between the molecules results in joining the molecules into a threedimensional laye

Reinvestigation of the synthesis of isoliquiritigenin: Application of Horner-Wadsworth-Emmons reaction and Claisen-Schmidt condensation

Sano, Shigeki,Okubo, Yoshinori,Handa, Atsushi,Nakao, Michiyasu,Kitaike, Syuji,Nagao, Yoshimitsu,Kakegawa, Hisao

scheme or table, p. 885 - 888 (2011/08/06)

Isoliquiritigenin [ILG, (E)-1] was readily prepared via the Horner-Wadsworth-Emmons reactions using β -ketophosphonates 5a, b. An improved protocol for the synthesis of (E)-1 via the Claisen-Schmidt condensation was also presented.

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