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63224-15-7

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63224-15-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63224-15-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,2,2 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 63224-15:
(7*6)+(6*3)+(5*2)+(4*2)+(3*4)+(2*1)+(1*5)=97
97 % 10 = 7
So 63224-15-7 is a valid CAS Registry Number.

63224-15-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[2-(dimethylamino)ethyl]propanamide

1.2 Other means of identification

Product number -
Other names N-(2-(Dimethylamino)ethyl)propanamide

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:63224-15-7 SDS

63224-15-7Relevant articles and documents

INFLUENCE OF THE CONFORMATION OF AMIDE ANALOGS OF ACETYLCHOLINE ON THEIR CHOLINOMIMETIC ACTIVITY

Khromov-Borisov, N. V.,Aleksandrova, L. N.,Danilov, A. F.,Shelkovnikov, S. A.

, p. 401 - 403 (1984)

-

A Simple Aliphatic Diamine Auxiliary for Palladium-Catalyzed Arylation of Unactivated β-C(sp3)-H Bonds

Lou, Jiang,Wang, Quannan,He, Yuan,Yu, Zhengkun

supporting information, p. 4571 - 4584 (2018/10/25)

Palladium-catalyzed β-C(sp3)-H arylation of aliphatic acid derivatives was achieved by means of 2-dimethylaminoethylamine auxiliary as a directing group. The β-C(sp3)-H arylation reactions with aryl and heteroaryl iodides efficiently afforded the corresponding arylated hydrocinnamic acid derivatives. Direct β-C(sp3)-H alkynylation, and arene C?H arylation and alkynylation were also realized under the same or slightly modified conditions. The aliphatic diamine auxiliary in the products could be readily removed by methanol in the presence of BF3 ? OEt2. In comparison with the widely used bidentate nitrogen-containing directing groups, 2-dimethylaminoethylamine is a simple, cheap, readily available and removable, and atom-economical directing group for C?H functionalization. (Figure presented.).

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