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Benzamide, N-propoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64648-16-4

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64648-16-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64648-16-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,6,4 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 64648-16:
(7*6)+(6*4)+(5*6)+(4*4)+(3*8)+(2*1)+(1*6)=144
144 % 10 = 4
So 64648-16-4 is a valid CAS Registry Number.

64648-16-4SDS

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 N-propoxybenzamide

1.2 Other means of identification

Product number -
Other names N-propoxy-benzamide

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:64648-16-4 SDS

64648-16-4Relevant academic research and scientific papers

Copper-catalyzed C-N bond formation through C-H/N-H activation: A novel approach to the synthesis of multisubstituted ureas

Jiang, Honglai,Lin, Aijun,Zhu, Chengjian,Cheng, Yixiang

supporting information, p. 819 - 821 (2013/02/23)

A copper-catalyzed cross-dehydrogenative coupling reaction that involves C-H activation of formamides and N-H activation of N-alkoxy amides has been developed. This protocol affords a novel approach to the synthesis of multisubstituted ureas under mild co

Reactions of N-Acyl-O-arylhydroxylamines: Part IV - Preparation of Some N-Arylsulphonyl-O-arylhydroxylamines

Singha, A. S.,Misra, B. N.

, p. 361 - 363 (2007/10/02)

A number of N-arylsulphonyl-O-alkylhydroxylamines (III) have been prepared by condensing appropriate alkoxyamines with arylsulphonyl chlorides in the presence of a base.The alkoxyamines have been obtained from the corresponding alkoxyamine hydrochlorides or hydrobromides (II) which in turn have been prepared by the hydrolysis of appropriate N-benzoyl-O-alkylhydroxylamines (I) with ethanolic hydrogen chloride or hydrogen bromide.The structure assignments of III are based on elemental analyses, chemical reaction and spectral (IR, PMR) data.

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