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104296-15-3

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104296-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104296-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,2,9 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 104296-15:
(8*1)+(7*0)+(6*4)+(5*2)+(4*9)+(3*6)+(2*1)+(1*5)=103
103 % 10 = 3
So 104296-15-3 is a valid CAS Registry Number.

104296-15-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethoxy-1-iodonaphthalene

1.2 Other means of identification

Product number -
Other names 1-iodo-2-ethoxynaphthalene

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:104296-15-3 SDS

104296-15-3Downstream Products

104296-15-3Relevant articles and documents

-

Corral,Orazi

, p. 11,15 (1956)

-

One-pot preparation of arylalkynes by a tandem catalytic iodination of arenes and palladium-catalyzed coupling of iodoarenes with terminal alkynes

Wan, Shun,Wang, Sunewang R.,Lu, Wenjun

, p. 4349 - 4352 (2006)

Iodination of activated arenes by air-oxidation is carried out in the presence of catalytic bismuth salts at room temperature. Subsequently, the formed iodoarenes react with terminal alkynes to give arylalkynes under a selected palladium-catalyzed coupling condition in the same pot.

Aromatic iodination of activated arenes and heterocycles with lead tetraacetate as the oxidant

Krassowska-Swiebocka,Lulinski,Skulski

, p. 926 - 928 (2007/10/02)

An easy, cheap and fairly quick laboratory method is presented for aromatic iodination of some highly activated arenes and heterocycles with molecular iodine in the presence of either pure lead tetraacetate dissolved in glacial acetic acid, or with the same oxidant but prepared in situ from Pb3O4 dissolved in hot AcOH/Ac2O prior to the iodination. 4-Bromo- and 2,4-dibromoanisoles are obtained from anisole by the respective oxidative bromination.

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