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1084-26-0

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1084-26-0 Usage

General Description

1-(4-tert-butyl-phenyl)-pyrrole-2,5-dione, also known as PTBPD, is a chemical compound with a molecular formula C15H15NO2. It is a pyrrole-2,5-dione derivative with a tert-butyl phenyl group attached to the pyrrole ring. PTBPD is commonly used in organic synthesis and has potential applications in pharmaceuticals, materials science, and organic electronics. It has been studied for its anti-inflammatory and antioxidant properties, as well as for its potential as a building block for novel organic materials. PTBPD may also have applications in the development of new dyes, pigments, and polymers due to its unique chemical structure and reactivity. Due to its versatility and potential uses, PTBPD is a compound of interest for researchers in various fields of science and technology.

Check Digit Verification of cas no

The CAS Registry Mumber 1084-26-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,8 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1084-26:
(6*1)+(5*0)+(4*8)+(3*4)+(2*2)+(1*6)=60
60 % 10 = 0
So 1084-26-0 is a valid CAS Registry Number.

1084-26-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-tert-butylphenyl)pyrrole-2,5-dione

1.2 Other means of identification

Product number -
Other names -

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

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More Details:1084-26-0 SDS

1084-26-0Relevant articles and documents

Sterically controlled, palladium-catalyzed intermolecular amination of arenes

Shrestha, Ruja,Mukherjee, Paramita,Tan, Yichen,Litman, Zachary C.,Hartwig, John F.

supporting information, p. 8480 - 8483 (2013/07/19)

We report the Pd-catalyzed amination of arenes to form N-aryl phthalimides with regioselectivity controlled predominantly by steric effects. Mono-, di-, and trisubstituted arenes lacking a directing group undergo amination reactions with moderate to high yields and high regioselectivities from sequential addition of PhI(OAc)2 as an oxidant in the presence of Pd(OAc) 2 as catalyst. This sterically derived selectivity contrasts that for analogous arene acetoxylation.

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