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Pentanamide, 4,4-dimethyl-N-2-pyridinyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

579470-27-2

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579470-27-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 579470-27-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,9,4,7 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 579470-27:
(8*5)+(7*7)+(6*9)+(5*4)+(4*7)+(3*0)+(2*2)+(1*7)=202
202 % 10 = 2
So 579470-27-2 is a valid CAS Registry Number.

579470-27-2SDS

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 N-(2-pyridyl)-4,4-dimethyl pentanamide

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:579470-27-2 SDS

579470-27-2Downstream Products

579470-27-2Relevant academic research and scientific papers

Ru-catalyzed hydroamidation of alkenes and cooperative aminocarboxylation procedure with chelating formamide

Ko, Sangwon,Han, Hoon,Chang, Sukbok

, p. 2687 - 2690 (2003)

(Matrix presented) A strategy of chelation-assisted activation of formamide was employed to achieve hydroamidation of alkenes to generate one-carbon-elongated amides in moderate to good selectivity and yields. Also reported is the two-metal-catalyzed cooperative aminocarboxylation of aryl iodides, in which Ru is presumed to catalyze decarbonylation of formamide to release carbon monoxide and amine for the subsequent Pd-catalyzed aminocarboxylation routes, thus enabling the net transformation to be performed in the absence of external CO pressure.

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