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2-Butenoic acid, 4-(2-iodophenyl)-, ethyl ester, (2E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

452055-90-2

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452055-90-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 452055-90-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,2,0,5 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 452055-90:
(8*4)+(7*5)+(6*2)+(5*0)+(4*5)+(3*5)+(2*9)+(1*0)=132
132 % 10 = 2
So 452055-90-2 is a valid CAS Registry Number.

452055-90-2SDS

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 ethyl (E)-4-(2-iodophenyl)-2-butenoate

1.2 Other means of identification

Product number -
Other names ethyl (E)-4-(2-iodophenyl)but-2-enoate

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:452055-90-2 SDS

452055-90-2Downstream Products

452055-90-2Relevant academic research and scientific papers

Intramolecular [1 + 2] and [3 + 2] cycloaddition reactions of cyclopropenone ketals

Patel, Paresma R.,Boger, Dale L.

supporting information; experimental part, p. 8527 - 8529 (2010/08/06)

The first intramolecular thermal reactions of cyclopropenone ketals are reported and the work examined substrates tethered to an electron-deficient olefin bearing a single electron-withdrawing substituent. Whereas the intermolecular variants of the reacti

Synthesis of substituted naphthalenes by the palladium-catalyzed annulation of internal alkynes

Huang, Qinhua,Larock, Richard C.

, p. 2505 - 2508 (2007/10/03)

(Matrix presented) A variety of substituted naphthalenes have been prepared by the palladium-catalyzed carboannulation of internal alkynes. This method (1) forms two new carbon-carbon bonds in a single step, (2) accommodates a variety of functional groups

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