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[Pd(anisyl)((ferrocenyl)di(tert-butyl)phosphine)(bis(3,5-bis(trifluoromethyl)phenyl)amide)] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

700378-54-7

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700378-54-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 700378-54-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,0,3,7 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 700378-54:
(8*7)+(7*0)+(6*0)+(5*3)+(4*7)+(3*8)+(2*5)+(1*4)=137
137 % 10 = 7
So 700378-54-7 is a valid CAS Registry Number.

700378-54-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [Pd(anisyl)((ferrocenyl)di(tert-butyl)phosphine)(bis(3,5-bis(trifluoromethyl)phenyl)amide)]

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:700378-54-7 SDS

700378-54-7Upstream product

700378-54-7Relevant academic research and scientific papers

Synthesis, Structure, and Reductive Elimination Chemistry of Three-Coordinate Arylpalladium Amido Complexes

Yamashita, Makoto,Hartwig, John F.

, p. 5344 - 5345 (2004)

Four three-coordinate arylpalladium amido complexes with a single hindered phosphine were isolated and structurally characterized. Each possessed a T-shaped geometry. Several of these complexes possessed true three-coordinate structures that lacked any additional coordination by ligand C-H bonds. All of the three-coordinate complexes underwent reductive elimination to form the corresponding triarylamine. A comparison of the rate of reaction of the three-coordinate compounds demonstrated that the rate of elimination from the pentaphenylferrocenyl di-tert-butylphosphine complex were the fastest. A comparison of the rates of reactions between three-coordinate and four-coordinate complexes showed that the rates were much faster from the three-coordinate complexes. Copyright

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