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1,4-Epoxynaphthalene, 6,7-dichloro-1,4-dihydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

144474-60-2

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144474-60-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144474-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,4,7 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 144474-60:
(8*1)+(7*4)+(6*4)+(5*4)+(4*7)+(3*4)+(2*6)+(1*0)=132
132 % 10 = 2
So 144474-60-2 is a valid CAS Registry Number.

144474-60-2SDS

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 6,7-Dichloro-1,4-dihydro-1,4-epoxynaphthalene

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:144474-60-2 SDS

144474-60-2Downstream Products

144474-60-2Relevant academic research and scientific papers

Reaction of 1,2-dihalogen substituted arenes with lanthanum metal: A new generation method of benzyne

Kawabata, Hiroshi,Nishino, Toshiki,Nishiyama, Yutaka,Sonoda, Noboru

, p. 4911 - 4913 (2002)

A new generation method of benzyne has been developed. When 1,2-dihalogen substituted arenes were allowed to react with lanthanum metal in the presence of dienes, Diels-Alder products between benzyne and dienes were formed in moderate to good yields.

Dehalogenation of o-dihalogen substituted arenes and α,α′-dihalogen substituted o-xylenes with lanthanum metal

Nishiyama, Yutaka,Kawabata, Hiroshi,Nishino, Toshiki,Hashimoto, Kouji,Sonoda, Noboru

, p. 6609 - 6614 (2007/10/03)

It was found that lanthanum metal caused the dehalogenation of o-dihalogen substituted arenes and α,α′-dihalogen substituted o-xylenes to generate the corresponding benzynes and o-quinodimethanes. When o-dihalogen substituted arenes were allowed to react with lanthanum metal in the presence of dienes, the Diels-Alder products between benzyne and dienes were formed in moderate to good yields. Similarly, the Diels-Alder adducts of o-quinodimethane with dienophiles were obtained, in the reaction of α,α′-dibromo-o-xylenes with lanthanum metal in the presence of dienophiles.

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