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2-chloro-N-methyl-N-phenylpropanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64754-68-3

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64754-68-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64754-68-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,7,5 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 64754-68:
(7*6)+(6*4)+(5*7)+(4*5)+(3*4)+(2*6)+(1*8)=153
153 % 10 = 3
So 64754-68-3 is a valid CAS Registry Number.

64754-68-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-N-methyl-N-phenylpropanamide

1.2 Other means of identification

Product number -
Other names 2-Chlor-propionsaeure-(N-methyl-anilid)

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:64754-68-3 SDS

64754-68-3Relevant academic research and scientific papers

Transfer Hydro-dehalogenation of Organic Halides Catalyzed by Ruthenium(II) Complex

You, Tingjie,Wang, Zhenrong,Chen, Jiajia,Xia, Yuanzhi

, p. 1340 - 1346 (2017/02/10)

A simple and efficient Ru(II)-catalyzed transfer hydro-dehalogenation of organic halides using 2-propanol solvent as the hydride source was reported. This methodology is applicable for hydro-dehalogenation of a variety of aromatic halides and α-haloesters and amides without additional ligand, and quantitative yields were achieved in many cases. The potential synthetic application of this method was demonstrated by efficient gram-scale transformation with catalyst loading as low as 0.5 mol %.

Stereoconvergent amine-directed alkyl-alkyl Suzuki reactions of unactivated secondary alkyl chlorides

Lu, Zhe,Wilsily, Ashraf,Fu, Gregory C.

supporting information; experimental part, p. 8154 - 8157 (2011/07/08)

A new family of stereoconvergent cross-couplings of unactivated secondary alkyl electrophiles has been developed, specifically, arylamine-directed alkyl-alkyl Suzuki reactions. This represents the first such investigation to be focused on the use of alkyl

A New and Practical Synthesis of Indolones

Boivin, Jean,Yousfi, Mohammed,Zard, Samir Z.

, p. 9553 - 9556 (2007/10/02)

A variety of indolones can be obtained from α-haloanilides through a radical cyclisation mediated by a combination of nickel powder and acetic acid.

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