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1,5-DICHLORO-9-METHYL-ANTHRACENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27532-80-5

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27532-80-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27532-80-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,5,3 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27532-80:
(7*2)+(6*7)+(5*5)+(4*3)+(3*2)+(2*8)+(1*0)=115
115 % 10 = 5
So 27532-80-5 is a valid CAS Registry Number.

27532-80-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,5-dichloro-9-methylanthracene

1.2 Other means of identification

Product number -
Other names 1,5-Dichlor-9-methyl-anthracen

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:27532-80-5 SDS

27532-80-5Downstream Products

27532-80-5Relevant academic research and scientific papers

Reactions of Copper(II) Halides with Aromatic Compounds. Part XII. Reactions of 9-Methyl-10-phenylanthracene, 1,4,9-Trimethylanthracene, 9,10-Dimethylanthracene and 1,5-Dichloro-9-methylanthracene in Methanol.

Mancilla, Jerson M.,Nonhebel, Derek C.,Scullion, Ian

, p. 1601 - 1619 (2007/10/02)

The title compounds react with copper(II) bromide in methanol to give the corresponding 9-methoxymethyl compounds. 1,4,9-Trimethylanthracene and 1,5-dichloro-9-methylanthracene also gave 1,2-di-(1,4-dimethyl-9-anthryl)ethane (6) and 1,5-dichloro-9,10-dimethoxy-9,10-dihydroanthracene (9) respectively.The formation of all these products can be interpreted in terms of initial electron transfer oxidation of the substituted anthracene to its radical cation, which either subsequently loses a proton to give the substituted 9-anthrylmethyl radical or undergoes solvent capture.

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