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2(1H)-Naphthalenone, 1,1-bis(benzoyloxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13302-29-9

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13302-29-9 Usage

Physical form

White powder

Type of compound

Organic peroxide

Uses

+ Radical initiator in the polymerization of acrylic and vinyl monomers, used in the production of plastics, adhesives, and coatings
+ Key ingredient in acne treatments and hair bleaching products

Functionality

Effectively kills bacteria and promotes skin exfoliation

Risks

+ Strong oxidizing agent
+ Can cause skin irritation and allergic reactions in some individuals
+ Must be handled with care and caution

Check Digit Verification of cas no

The CAS Registry Mumber 13302-29-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,0 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13302-29:
(7*1)+(6*3)+(5*3)+(4*0)+(3*2)+(2*2)+(1*9)=59
59 % 10 = 9
So 13302-29-9 is a valid CAS Registry Number.

13302-29-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (1-benzoyloxy-2-oxonaphthalen-1-yl) benzoate

1.2 Other means of identification

Product number -
Other names -

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:13302-29-9 SDS

13302-29-9Relevant academic research and scientific papers

The Oxidation of Some Naphthols with Benzoyl Peroxide

Matsumoto, Takashi,Imai, Sachihiko,Yamamoto, Naoya

, p. 911 - 920 (1988)

The reactions of four naphthols (1-naphthol (1), 2-naphthol (2), 4-isopropyl-1-naphthol (18), and 3-isopropyl-2-naphthol (19)) with benzoyl peroxide were examined under two reaction conditions (A and B).Each of the naphthols 1,2,18, and 19 was oxidized wi

Dearomatisation of 2-Naphthol by Oxidative Nucleophilic Substitution: an Efficient Two-step Process

Barton, Derek H.R.,Berge-Lurion, Reine-Marie,Lusinchi, Xavier,Pinto, B. Mario

, p. 2077 - 2080 (2007/10/02)

An efficient synthesis of 1,1-dimethoxynaphthalen-2(1H)-one (13) has been achieved.Oxidation of 2-naphthol with bis-p-nitrobenzoyl peroxide gave the known derivative (5).Methylation with diazomethane and hydrolysis afforded 1-methoxy-2-naphthol which was

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