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BIS-(3-ACETYL-4-HYDROXYPHENYL)-METHANE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28467-22-3

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28467-22-3 Usage

Preparation

Obtained by Fries rearrangement of 4,4′-diacetoxy-diphenylmethane, ? with aluminium chloride at 130–140° for 1 h (50%) ; ? with aluminium chloride and sodium chloride mixture at 140–150° for 4 h (28%).

Check Digit Verification of cas no

The CAS Registry Mumber 28467-22-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,4,6 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 28467-22:
(7*2)+(6*8)+(5*4)+(4*6)+(3*7)+(2*2)+(1*2)=133
133 % 10 = 3
So 28467-22-3 is a valid CAS Registry Number.
InChI:InChI=1/C17H16O4/c1-10(18)14-8-12(3-5-16(14)20)7-13-4-6-17(21)15(9-13)11(2)19/h3-6,8-9,20-21H,7H2,1-2H3

28467-22-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[5-[(3-acetyl-4-hydroxyphenyl)methyl]-2-hydroxyphenyl]ethanone

1.2 Other means of identification

Product number -
Other names Bis-(3-acetyl-4-hydroxyphenyl)-methane

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:28467-22-3 SDS

28467-22-3Downstream Products

28467-22-3Relevant academic research and scientific papers

Crystallization-induced light-emission enhancement of diphenylmethane derivatives

Guieu, Samuel,Rocha, Jo?o,Silva, Artur M.S.

, p. 9329 - 9334 (2013/10/01)

A family of diphenylmethane derivatives has been synthesized and their luminescence properties characterized. While in solution the compounds are weakly emissive, showing no aggregation-induced emission enhancement, the crystals of three dialkyl 5,5′-methylenebis(2-hydroxybenzoate) samples exhibit intense emission. This emission enhancement upon crystallization is ascribed to particular molecular packing, which stiffens the structure of the compounds via hydrogen bonds, preventing consecutive π-π interactions.

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