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2675-88-9

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2675-88-9 Usage

Uses

n,2-Dimethylpropanamide can be used to treat, inhibit, or prevent plant pathogenic disease.

Synthesis Reference(s)

The Journal of Organic Chemistry, 30, p. 2376, 1965 DOI: 10.1021/jo01018a063

Check Digit Verification of cas no

The CAS Registry Mumber 2675-88-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,7 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2675-88:
(6*2)+(5*6)+(4*7)+(3*5)+(2*8)+(1*8)=109
109 % 10 = 9
So 2675-88-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H11NO/c1-4(2)5(7)6-3/h4H,1-3H3,(H,6,7)

2675-88-9SDS

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,2-dimethylpropanamide

1.2 Other means of identification

Product number -
Other names Propanamide,N,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:2675-88-9 SDS

2675-88-9Downstream Products

2675-88-9Relevant articles and documents

-

Allred,E.L.,Hurwitz,M.D.

, p. 2376 - 2381 (1965)

-

Cationic Carbon to Nitrogen Rearrangements in the Reactions of N-(Sulfonyloxy)amines with Aldehydes

Hoffman, Robert V.,Salvador, James M.

, p. 4487 - 4490 (2007/10/02)

A series of aromatic and aliphatic aldehydes was reacted with N-((p-nitrobenzenesulfonyl)oxy)methylamine in chloroform.Products resulting from both carbon migration and hydride migration to nitrogen were isolated.The ratios of carbon to hydride migration products were used to clarify the reaction mechanism.The results support a two-step process in which cationic carbon to nitrogen rearrangements is rate determining.

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