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628333-84-6

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628333-84-6 Usage

Chemical structure

The compound consists of a pyrazole ring with two phenyl groups attached at positions 3 and 5, and a phosphino group attached at position 2 of the pyrazole ring.

Phosphino group substitution

The phosphino group is further substituted with two isopropyl groups.

Potential applications

It is a potential ligand in coordination chemistry and catalysis.

Synthesis utility

It can be used in the synthesis of organic compounds and materials.

Unique structure

Its unique structure and properties make it an interesting candidate for further research in various fields.

Research potential

Due to its unique structure and potential applications, it is a promising compound for further research in the fields of chemistry, materials science, and catalysis.

Check Digit Verification of cas no

The CAS Registry Mumber 628333-84-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,8,3,3 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 628333-84:
(8*6)+(7*2)+(6*8)+(5*3)+(4*3)+(3*3)+(2*8)+(1*4)=166
166 % 10 = 6
So 628333-84-6 is a valid CAS Registry Number.

628333-84-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(3,5-diphenylpyrazol-1-yl)phenyl]-di(propan-2-yl)phosphane

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:628333-84-6 SDS

628333-84-6Downstream Products

628333-84-6Relevant articles and documents

Alternative biarylphosphines for use in the palladium-catalyzed amination of aryl halides

Singer, Robert A.,Caron, Stephane,McDermott, Ruth E.,Arpin, Patrice,Do, Nga M.

, p. 1727 - 1731 (2007/10/03)

Two families of biarylphosphine ligands were prepared for use in the Pd-catalyzed amination reaction. The first series investigated was derived from N-phenylpyrroles, and the second, was derived from N-phenylpyrazoles. While the pyrrole ligands were not as general in substrate scope, one of the readily prepared pyrazole ligands (R = t-Bu) was found to have a fairly broad substrate scope.

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