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N-phenyl-4-(prop-1-en-2-yl)aniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65036-78-4

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65036-78-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65036-78-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,0,3 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 65036-78:
(7*6)+(6*5)+(5*0)+(4*3)+(3*6)+(2*7)+(1*8)=124
124 % 10 = 4
So 65036-78-4 is a valid CAS Registry Number.

65036-78-4SDS

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 phenyl-l<sup>3</sup>-iodanediyl bis(2,4,6-trimethylbenzoate)

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:65036-78-4 SDS

65036-78-4Downstream Products

65036-78-4Relevant academic research and scientific papers

Buchwald-Hartwig amination of (hetero)aryl chlorides by employing Mor-DalPhos under aqueous and solvent-free conditions

Tardiff, Bennett J.,Stradiotto, Mark

experimental part, p. 3972 - 3977 (2012/08/27)

We report on the application of the [Pd(cinnamyl)Cl]2/Mor- DalPhos catalyst system in the Buchwald-Hartwig amination of (hetero)aryl chlorides with primary or secondary amines conducted either under aqueous conditions without the use of co-solvents and/or surfactants or under solvent-free conditions (52 examples). We have established that reactions of this type can be conducted without the rigorous exclusion of air, and in the case of the solvent-free reactions, we have demonstrated that appropriately selected liquid and solid reagents can be employed successfully.

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