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Benzofuran, 3-(2-iodophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

452962-66-2

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452962-66-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 452962-66-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,2,9,6 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 452962-66:
(8*4)+(7*5)+(6*2)+(5*9)+(4*6)+(3*2)+(2*6)+(1*6)=172
172 % 10 = 2
So 452962-66-2 is a valid CAS Registry Number.

452962-66-2SDS

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 3-(2-iodophenyl)-1-benzofuran

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:452962-66-2 SDS

452962-66-2Relevant academic research and scientific papers

Novel 1,4-palladium migration in organopalladium intermediates derived from o-lodobiaryls

Campo, Marino A.,Larock, Richard C.

, p. 14326 - 14327 (2002)

A novel 1,4-palladium migration in organopalladium intermediates derived from o-iodobiaryls has been observed under modified Heck reaction conditions. This migration process can be switched "on" or "off" by simply choosing the appropriate reaction conditi

Intramolecular Electrophilic Cyclization Approach to 6-Substituted Naphtho[2,1- b]benzofurans: Novel Dual-State Emissive Fluorophores with Blue Emission

Singh, Dileep Kumar,Jang, Kyungkuk,Kim, Jinhwang,Lee, Jeeyeon,Kim, Ikyon

supporting information, p. 408 - 416 (2019/05/01)

A regiospecific synthesis of naphtho[2,1-b]benzofurans with a substituent at the C6 position was achieved via intramolecular 6-endo-dig electrophilic cyclization under acidic conditions to construct the central aromatic C ring. Screening of the synthesize

Synthesis of fluoren-9-ones by the palladium-catalyzed cyclocarbonylation of o-halobiaryls

Campo, Marino A.,Larock, Richard C.

, p. 5616 - 5620 (2007/10/03)

The synthesis of various substituted fluoren-9-ones has been accomplished by the palladium-catalyzed cyclocarbonylation of o-halobiaryls. The cyclocarbonylation of 4′-substituted 2-iodobiphenyls produces very high yields of 2-substituted fluoren-9-ones bearing either electron-donating or electron-withdrawing substituents. 3′-Substituted 2-iodobiphenyls afford 3-substituted fluoren-9-ones in excellent yields with good regioselectivity. This chemistry has been successfully extended to polycyclic fluorenones and fluorenones containing fused isoquinoline, indole, pyrrole, thiophene, benzothiophene, and benzofuran rings.

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