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4-Pentenal, 3-methylene-5-phenyl-, (4E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

204570-75-2

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204570-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 204570-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,5,7 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 204570-75:
(8*2)+(7*0)+(6*4)+(5*5)+(4*7)+(3*0)+(2*7)+(1*5)=112
112 % 10 = 2
So 204570-75-2 is a valid CAS Registry Number.

204570-75-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylidene-5-phenylpent-4-enal

1.2 Other means of identification

Product number -
Other names 3-methylene-5-phenyl-pent-4-enal

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:204570-75-2 SDS

204570-75-2Relevant academic research and scientific papers

New synthetic analogs of retinoids: Synthesis of aromatic analogs of 9-methylidene- and 13-demethyl-9-methylidene-retinol, -retinal, and ethyl 13-demethyl-9-methylideneretinoate

Valla, Alain,Prat, Virginie,Laurent, Alain,Andriamialisoa, Zo,Cartier, Dominique,Giraud, Michel,Labia, Roger,Potier, Pierre

, p. 3423 - 3427 (2007/10/03)

Aromatic analogs of 9-methylidene and 13-demethyl-9-methylideneretinol, -retinal, and ethyl 13-demethyl-9-methylideneretinoate were synthesized via a new β-methylidene-aldehyde synthon.

Ene diiodo acetals: Stereoselective synthesis of ene hydroxy acetals. Handy access to non conjugated dienals

Bonnet,Ple,Duhamel

, p. 2743 - 2752 (2007/10/03)

After halogen-metal exchange reaction followed by condensation with carbonyl compounds, ene diiodo acetal 1 allow the stereoselective synthesis of ene hydroxy acetals 2 with Z configuration, in a two step procedure. Moreover, after dehydration, the intermediate diene acetals 3-4, via an appropriated hydrolysis procedure, lead to pure non conjugated dienals 5.

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