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140709-06-4

140709-06-4

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140709-06-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 140709-06-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,7,0 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 140709-06:
(8*1)+(7*4)+(6*0)+(5*7)+(4*0)+(3*9)+(2*0)+(1*6)=104
104 % 10 = 4
So 140709-06-4 is a valid CAS Registry Number.

140709-06-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-naphthalen-1-yl-N,N-di(propan-2-yl)acetamide

1.2 Other means of identification

Product number -
Other names N,N-DIISOPROPYL-NAPHTHALEN-1-YLACETAMIDE

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:140709-06-4 SDS

140709-06-4Relevant articles and documents

Charge-Transfer Complex Promoted C-N Bond Activation for Ni-Catalyzed Carbonylation

Yu, Hui,Gao, Bao,Hu, Bin,Huang, Hanmin

supporting information, p. 3520 - 3523 (2017/07/17)

A new strategy was developed for activation of C-N bond via formation of an amine-I2 charge-transfer complex, which facilitates the inert C-N bond activation via oxidative addition with Ni(0). This strategy has been successfully applied in the Ni-catalyzed carbonylation of benzylamines via direct insertion of CO into the C-N bond, which provided a straightforward and rapid approach to arylacetamides in the presence of catalytic amounts of I2 and Ni catalyst. Mechanistic studies suggested that a benzyl radical generated via the oxidative addition was involved in the present reaction.

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