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2-Propenoic acid, 2,3-diiodo-3-phenyl-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66288-38-8

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66288-38-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66288-38-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,8 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 66288-38:
(7*6)+(6*6)+(5*2)+(4*8)+(3*8)+(2*3)+(1*8)=158
158 % 10 = 8
So 66288-38-8 is a valid CAS Registry Number.

66288-38-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-diiodo-3-phenylprop-2-enoic acid

1.2 Other means of identification

Product number -
Other names 2-Propenoic acid,2,3-diiodo-3-phenyl-,(E)

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:66288-38-8 SDS

66288-38-8Relevant academic research and scientific papers

Selective synthesis of dihalo-substituted unsaturated carboxylic acids and derivatives

Langle, Sandrine,Ngi, Samuel Inack,Anselmi, Elsa,Abarbri, Mohamed,Thibonnet, Jerome,Duchene, Alain

, p. 1724 - 1728 (2008/02/05)

A selective one-pot procedure was developed for the production of E-dihalo-substituted α,β-unsaturated alkenoic acids and derivatives from the corresponding α,β-unsaturated alkynoic acids. Georg Thieme Verlag Stuttgart.

Heterocyclization of Substituted Phenylpropynoic Acids by the Action of Selenium Dioxide and Hydrogen Halides

Zborovskii,Levon,Staninets

, p. 1798 - 1801 (2007/10/03)

Heterocyclization of phenylpropynoic acid and its derivatives by the action of selenium dioxide and hydrogen halides proceeds through intermediate formation of selenium tetrahalides and yields benzo[b]-selenophene derivatives. Substituents in the benzene

Oxidative Decarboxylation of Propiolic Acids

Cohen, Mark J.,McNelis, Edward

, p. 515 - 518 (2007/10/02)

The combination of iodine and iodine pentoxide in methanol was used to convert phenylpropiolic acid and 2-hexynoic acid to the corresponding ketal esters of one less carbon.In both cases, iodoacetylenic compounds were shown to be intermediates.In the case of the phenylpropiolic acid, a diiodoalkene was isolated and shown to be a second intermediate.

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