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N-allylsalicylamide, with the molecular formula C10H11NO2, is a versatile chemical compound derived from salicylamide, which is known for its analgesic and antipyretic properties. N-allylsalicylamide plays a significant role in the field of polymer chemistry and materials science due to its various applications.

118-62-7

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118-62-7 Usage

Uses

Used in Polymer Synthesis:
N-allylsalicylamide is utilized as a monomer in the synthesis of thermosetting polymers, which are crucial in the production of adhesives and resins. Its incorporation into these materials contributes to their enhanced performance characteristics.
Used in Crosslinking Agent Applications:
As a crosslinking agent, N-allylsalicylamide is employed to strengthen various polymer systems. Its use results in the improvement of the mechanical and thermal properties of the final materials, making them more robust and suitable for a range of applications.
Used in Corrosion Inhibition:
N-allylsalicylamide has been investigated for its potential as a corrosion inhibitor in aqueous systems. This application could be particularly beneficial in industries where the prevention of metal corrosion is essential for maintaining the integrity and longevity of equipment and structures.

Check Digit Verification of cas no

The CAS Registry Mumber 118-62-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 118-62:
(5*1)+(4*1)+(3*8)+(2*6)+(1*2)=47
47 % 10 = 7
So 118-62-7 is a valid CAS Registry Number.

118-62-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-N-prop-2-enylbenzamide

1.2 Other means of identification

Product number -
Other names Salicylamide,N-allyl

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:118-62-7 SDS

118-62-7Relevant academic research and scientific papers

Efficient synthesis of 16-28 membered macrocyclic crown amides via ring closing metathesis

Ibrahim, Yehia A.,Behbehani, Haider,Ibrahim, Maher R.,Malhas, Rana N.

, p. 7273 - 7282 (2003)

Ring closing metathesis of suitable diamides containing 1,ω-dienes led to efficient synthetic approaches towards macrocylic polyoxadiamides 1-18 with 16-28 membered ring sizes in good to excellent yields using Grubbs' catalyst.

Smiles rearrangements in Ugi- and Passerini-type couplings: New multicomponent access to O- and N-arylamides

El Kaim, Laurent,Gizolme, Marie,Grimaud, Laurence,Obie, Julie

, p. 4169 - 4180 (2007)

(Chemical Equation Presented) The use of Smiles rearrangement in Ugi- and Passerini-type couplings with electron-deficient phenols allows very straightforward multicomponent formation of O-aryl- and N-arylamides. Best yields were observed with the highly activated o- and p-nitrophenols, salicylic derivatives giving adducts in lower yields. The scope of these new reactions is further increased by the successful couplings of heterocyclic phenols such as hydroxypyridines and hydroxypyrimidines.

Electrochemical Chalcogenation of β,γ-Unsaturated Amides and Oximes to Corresponding Oxazolines and Isoxazolines

Baidya, Mrinmay,De Sarkar, Suman,Mahanty, Kingshuk,Maiti, Debabrata,Mallick, Samrat

supporting information, (2020/02/04)

The current report represents a transition-metal-free synthesis of oxazoline and isoxazoline derivatives by a tandem electro-oxidative chalcogenation-cyclization process. Both C?Se and C?S bond-forming protocols were developed without using any external oxidant and the reaction was performed at room temperature, open to the air. Using this methodology, 29 substituted oxazoline and 16 substituted isoxazoline derivatives were synthesized with up to 91% isolated yield. (Figure presented.).

Fast synthesis of amides from ethyl salicylate under microwave radiation in a solvent-free system

Lima, Rafaely N.,Silva, Valdenizia R.,De Santos, Luciano,Bezerra, Daniel P.,Soares, Milena B. P.,Porto, André L. M.

, p. 56566 - 56574 (2017/12/26)

In this study, amide bond formation, one of the most important reactions in organic chemistry, it was evaluated using ethyl salicylate and ten different primary amines. Under the optimized experimental conditions, i.e. 60 °C, hexane, phenylboronic acid-PBA (15 mol%), boric acid-BA (15 mol%) or without catalyst-WC, using a hot-plate for 24 h, amides were obtained in excellent isolated yields (WC, 77-94% to S-Aa-Ad; PBA, 11-94% to S-Ae-Aj; and BA, 28-90% to S-Ae-Aj). The reaction employing CAL-B also permitted a moderate conversion for the production of amides S-Ae-Aj (3-42%). However, in our efforts to reduce the amide synthesis time (24 h), the reactions were performed in the presence of microwave-MW radiation using a free-solvent system [60 °C, PBA (15 mol%) or WC], which reduced the time of the reaction by 32-fold (45 min) and afforded nine amides (S-Aa-Ah and S-Aj) in 80-99% isolated yield and S-Ai in 23% yield. A cytotoxicity assay demonstrated that the amide S-Ag was capable of inhibiting four human tumor cell lines (MCF-7, HCT116, HepG2, and HL-60) with an IC50 ranging from 8.68 to 17.57 μg mL-1. In this study, MW radiation provided an attractive way for faster reactions, improved yields, and cleaner reactions, as well as the synthesis of amide S-Ag with cytotoxic activity.

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