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2-Propenoic acid, 2-iodophenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67264-21-5

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67264-21-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67264-21-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,2,6 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67264-21:
(7*6)+(6*7)+(5*2)+(4*6)+(3*4)+(2*2)+(1*1)=135
135 % 10 = 5
So 67264-21-5 is a valid CAS Registry Number.

67264-21-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-iodophenyl acrylate

1.2 Other means of identification

Product number -
Other names 2-IC6H4(OC(O)CHCH2)

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:67264-21-5 SDS

67264-21-5Relevant academic research and scientific papers

Synthesis and radiofluorination of iodophenyl esters as tool for the traceless staudinger ligation

Pretze, Marc,Flemming, Anke,Koeckerling, Martin,Mamata, Constantin

, p. 1128 - 1136 (2011/01/09)

A new synthetic pathway for the preparation of ω-functionalized 2-iodophenyl esters as starting materials for the synthesis of substituted phosphanes is described. A radiolabeling of these esters with fluorine-18 has led to building blocks which were reacted with HPPh2 in a Pd-catalyzed P-C cross coupling to establish new phosphanes. These compounds can be applied as mild and bioorthogonal radiolabeling agents by means of the traceless Staudinger ligation. A route to access this class of compounds has been established.

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