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3-Chloro-2,2-dimethylpropanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41461-75-0

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41461-75-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41461-75-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,6 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 41461-75:
(7*4)+(6*1)+(5*4)+(4*6)+(3*1)+(2*7)+(1*5)=100
100 % 10 = 0
So 41461-75-0 is a valid CAS Registry Number.

41461-75-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-2,2-dimethylpropanamide

1.2 Other means of identification

Product number -
Other names Propanamide,3-chloro-2,2-dimethyl

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:41461-75-0 SDS

41461-75-0Relevant academic research and scientific papers

Pd-Catalyzed Directed Chlorination of Unactivated C(sp3)–H Bonds at Room Temperature

Xiong, Heng-Ying,Cahard, Dominique,Pannecoucke, Xavier,Besset, Tatiana

, p. 3625 - 3630 (2016/07/29)

A Pd-catalyzed directed chlorination of unactivated C(sp3)–H bonds has been developed. By using the bidentate 8-aminoquinolinyl directing group, selective chlorination of aliphatic amides has been achieved in moderate to good yields at room tem

METHOD FOR THE PREPARATION OF OMEGA-AMINO-ALKANEAMIDES AND OMEGA-AMINO-ALKANETHIOAMIDES AS WELL AS INTERMEDIATES OF THIS METHOD

-

Page/Page column 17-18, (2012/02/05)

The present invention relates to method for the preparation of an ω-amino-alkane(thio)amide having the formula (3). Furthermore, novel intermediates and partial reaction steps of the claimed method are disclosed.

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