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2,6-ditert-butyl-4-[(3,5-ditert-butyl-4-hydroxyphenyl)(phenyl)methylene]-2,5-cyclohexadien-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56523-92-3

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56523-92-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56523-92-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,5,2 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56523-92:
(7*5)+(6*6)+(5*5)+(4*2)+(3*3)+(2*9)+(1*2)=133
133 % 10 = 3
So 56523-92-3 is a valid CAS Registry Number.

56523-92-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Phenylgalvinol

1.2 Other means of identification

Product number -
Other names 2,6-Di-tert-butyl-4-[(3,5-di-tert-butyl-4-hydroxy-phenyl)-phenyl-methylene]-cyclohexa-2,5-dienone

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:56523-92-3 SDS

56523-92-3Relevant academic research and scientific papers

Elemental Sulfur-Promoted Synthesis of 4-Hydroxybenzophenones from p-Quinone Methides under Metal-Free Condition

Li, Jingping,Wang, Kunpeng,Wu, Jiayi,Zhang, Haoxiang,Chen, Yan,Liu, Qinglei,Xu, Junju,Yi, Weiyin

, (2022/05/20)

Conventional methods for the general and efficient synthesis of 4-hydroxybenzo- phenones are extremely underdeveloped and limited. We herein report a challenging metal-free protocol to rapidly construct 4-hydroxybenzophenones from para-quinone methides (p-QMs) in DMSO in the presence of KOH using the inexpensive and readily available elemental sulfur as redox reagent. As an unprecedented method, this simple but efficient approach has excellent site specificity, green sustainability, excellent atomic economy, and broad functional group compatibilities. Mechanistic studies show that the novel reaction proceeds through a radical pathway.

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