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Peroxide, bis(3-methoxybenzoyl), also known as bis(3-methoxybenzoyl) peroxide, is an organic compound with the chemical formula C16H14O6. It is a white crystalline solid that is commonly used as a catalyst and initiator in various chemical reactions, particularly in the polymerization of vinyl monomers and the curing of resins. This peroxide is derived from 3-methoxybenzoic acid and is characterized by its ability to decompose and release oxygen, which is useful in promoting the formation of polymer chains. It is also known for its stability and low volatility, making it a preferred choice in certain industrial applications. However, due to its reactivity, it requires careful handling and storage to prevent accidental decomposition and potential hazards.

1712-86-3

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1712-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1712-86-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,1 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1712-86:
(6*1)+(5*7)+(4*1)+(3*2)+(2*8)+(1*6)=73
73 % 10 = 3
So 1712-86-3 is a valid CAS Registry Number.

1712-86-3SDS

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 (3-methoxybenzoyl) 3-methoxybenzenecarboperoxoate

1.2 Other means of identification

Product number -
Other names m.m'-Dimethoxy-dibenzoylperoxyd

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:1712-86-3 SDS

1712-86-3Upstream product

1712-86-3Relevant academic research and scientific papers

Palladium(II)-catalyzed othro-C-H-benzoxylation of 2-arylpyridines by oxidative coupling with aryl acylperoxides

Sit, Wing-Nga,Chan, Chun-Wo,Yu, Wing-Yiu

, p. 4403 - 4418 (2013/05/22)

A palladium(II)-catalyzed ortho-benzoxylation of 2-arylpyridines with aryl acylperoxides was developed. With pyridyl as directing group, the benzoxylation reaction exhibits remarkable regioselectivity and excellent functional group tolerance, providing the products in up to 87% yield.

Palladium-catalyzed decarboxylative arylation of C-H bonds by aryl acylperoxides

Yu, Wing-Yiu,Sit, Wing Nga,Zhou, Zhongyuan,Chan, Albert S.-C.

supporting information; experimental part, p. 3174 - 3177 (2009/11/30)

A Pd(OAc)2-catalyzed protocol for decarboxylative arylation of aromatic C-H bond was developed using aryl acylperoxides as inexpensive aryl sources. Substrates containing pyridyl, oxime, and oxazoline groups undergo effectively ortho-selective C-H arylation with excellent functional group tolerance. This arylation should begin by directing-group-assisted cyclopalladation, followed by the reaction of the palladacycle with aryl radicals generated in situ by thermal decomposition of the peroxides.

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