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Benzenamine, N-(2-bromo-2-propenyl)-N-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60256-44-2

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60256-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60256-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,2,5 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60256-44:
(7*6)+(6*0)+(5*2)+(4*5)+(3*6)+(2*4)+(1*4)=102
102 % 10 = 2
So 60256-44-2 is a valid CAS Registry Number.

60256-44-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Methyl-N-phenyl-2-bromo-2-propenylamine

1.2 Other means of identification

Product number -
Other names N-(2-Bromoallyl)-N-methylaniline

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:60256-44-2 SDS

60256-44-2Relevant academic research and scientific papers

Enantioselective Palladium(II)-Catalyzed Intramolecular Aminoarylation of Alkenes by Dual N?H and Aryl C?H Bond Cleavage

Zhang, Wen,Chen, Pinhong,Liu, Guosheng

supporting information, p. 5336 - 5340 (2017/04/27)

An asymmetric palladium-catalyzed intramolecular oxidative aminoarylation of alkenes has been developed with quinoline–oxazoline chiral ligands and Ag2CO3 as the oxidant. Various indolines containing a quaternary stereogenic center were synthesized in high yield with excellent enantioselectivity. Preliminary mechanistic studies suggest that the addition of a catalytic amount of phenylglyoxylic acid significantly accelerates the reaction and slightly enhances the enantioselectivity.

Direct Coupling between β-Functionalized Organolithium Compounds and Aryl and Vinyl Halides

Barluenga, Jose,Montserrat, Javier M.,Florez, Josefa

, p. 6183 - 6186 (2007/10/02)

Treatment of N-lithio-N-(2-lithioethyl)benzamide with different aromatic and vinylic halides affords directly the corresponding substitution products: functionalized benzamides 3-10.

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