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47150-19-6

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47150-19-6 Usage

Chemical class

Pyrrole-2,5-dione derivatives

Versatile reactivity

Used in the synthesis of organic compounds and polymeric materials

Potential for functionalization

Can be modified to achieve desired properties

Agricultural applications

Exhibits fungicidal and antibacterial properties

Electronic and optical properties

Investigated for use in photovoltaic devices and organic light-emitting diodes (OLEDs)

Check Digit Verification of cas no

The CAS Registry Mumber 47150-19-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,7,1,5 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 47150-19:
(7*4)+(6*7)+(5*1)+(4*5)+(3*0)+(2*1)+(1*9)=106
106 % 10 = 6
So 47150-19-6 is a valid CAS Registry Number.

47150-19-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-tetradecylpyrrole-2,5-dione

1.2 Other means of identification

Product number -
Other names N-(n-Tetradecyl)-maleinsaeureimid

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:47150-19-6 SDS

47150-19-6Downstream Products

47150-19-6Relevant articles and documents

Uncovering new structural insights for antimalarial activity from cost-effective aculeatin-like derivatives

Winkler, Matthias,Maynadier, Marjorie,Wein, Sharon,Lespinasse, Marie-Ange,Boumis, Giovanna,Miele, Adriana E.,Vial, Henri,Wong, Yung-Sing

, p. 2064 - 2077 (2015/03/05)

A series of new aculeatin-like analogues were synthesized in two steps by combining two sets of building blocks. Many compounds showed inhibitory activities in vitro against Plasmodium falciparum and have helped to gain more insight into structure-activit

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