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

65993-49-9

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65993-49-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65993-49-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,9,9 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65993-49:
(7*6)+(6*5)+(5*9)+(4*9)+(3*3)+(2*4)+(1*9)=179
179 % 10 = 9
So 65993-49-9 is a valid CAS Registry Number.

65993-49-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-heptylprop-2-enamide

1.2 Other means of identification

Product number -
Other names N-heptyl-acrylamide

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:65993-49-9 SDS

65993-49-9Downstream Products

65993-49-9Relevant academic research and scientific papers

Effect of Hydrophobic Groups on Antimicrobial and Hemolytic Activity: Developing a Predictive Tool for Ternary Antimicrobial Polymers

Phuong, Pham Thu,Oliver, Susan,He, Junchen,Wong, Edgar H. H.,Mathers, Robert T.,Boyer, Cyrille

, p. 5241 - 5255 (2020/11/30)

Antimicrobial polymers have emerged as a potential solution to the growing problem of antimicrobial resistance. Although several studies have examined the effects of various parameters on the antimicrobial and hemolytic activity of statistical copolymers,

The phosphazo route to 2-alkenamides from acrylic acid and its derivatives

Cabral, Jose,Laszlo, Pierre,Montaufier, Marie-Therese,Lalatiana Randriamahefa

, p. 1705 - 1708 (2007/10/02)

2-Alkenamides are formed in good isolated yields (generally up to 70%) by the reaction of in situ-generated phosphazo compounds issued from aliphatic, alicyclic and aromatic primary amines, with acrylic acid and its derivatives.

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