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637-54-7

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637-54-7 Usage

General Description

Stearanilide is a chemical compound that is derived from stearic acid and aniline. It is commonly used as a lubricant and a slip agent in a variety of applications, including in the production of plastics and rubber. Stearanilide is also used as an anti-blocking agent in the manufacturing of polyolefin films and in the production of candles. It has a waxy white appearance and is odorless, making it suitable for use in various industrial and consumer products. Additionally, stearanilide is biodegradable and non-toxic, making it a relatively environmentally friendly option for use in many applications.

Check Digit Verification of cas no

The CAS Registry Mumber 637-54-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,3 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 637-54:
(5*6)+(4*3)+(3*7)+(2*5)+(1*4)=77
77 % 10 = 7
So 637-54-7 is a valid CAS Registry Number.
InChI:InChI=1/C24H41NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19-22-24(26)25-23-20-17-16-18-21-23/h16-18,20-21H,2-15,19,22H2,1H3,(H,25,26)

637-54-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-phenyloctadecanamide

1.2 Other means of identification

Product number -
Other names anilide of stearic acid

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:637-54-7 SDS

637-54-7Relevant articles and documents

Nano-Magnetic Sulfonic Acid Catalyzed Facile Synthesis of Diverse Amide Derivatives

Kothandapani, Jagatheeswaran,Ganesan, Asaithampi,Ganesan, Subramaniapillai Selva

, p. 685 - 692 (2017/01/25)

The excellent surface catalytic potential of Fe3O4-OSO3H is utilized in the synthesis of symmetrically and unsymmetrically substituted urea derivatives via transamidation reactions. The scope of the surface catalysis is further extended in transamidation reactions of cyclic and acyclic amide derivatives, and in the amidation of fatty acids. In both transamidation and amidation reactions, the catalyst is reusable up to five times without significant loss in its activity.

Cleavage of C-N bonds in guanidine derivatives and its relevance to efficient C-N bonds formation

Chang, Denghu,Zhu, Dan,Zou, Peng,Shi, Lei

, p. 1684 - 1693 (2015/03/30)

Efficient nonenzymatic decomposition of guanidine derivatives with high structural and functional diversity into anilide products is achieved in the presence of PdII/Cu(II) carboxylates/CO, relying on a dual C-N bonds cleavage strategy. In this decomposition process, the cooperative action of PdII species, Cu(II) carboxylates, and CO provides not only the N-acylating agents but also an initiator to trigger this C-N bonds cleavage sequence. The current results indicate that PdII/Cu(II) carboxylates/CO system provides a convenient and practical method for highly selective cleavage of unreactive C-N single bonds.

Total synthesis of monocyclic pyrimidinium betaines with fatty alkyl chains

Malki, Fatiha,Touati, Abdelkader,Rahal, Said,Moulay, Saad

scheme or table, p. 961 - 967 (2011/12/21)

Seven betaines were prepared by condensation of N,N'-diphenylamidines with malonic acid derivatives. The amidines were made via a multistep synthesis, starting from their corresponding fatty acids. Malonyl chloride and dipentachlorophenyl phenylmalonate, two derivatives of malonic acid, were obtained from malonic acid and benzyl chloride, respectively. Most of the products were characterized by IR, UV, 1H and 13C NMR. Biological assays of the synthesized betaines revealed their good antibacterial and antifungal activities against the Pseudomonas aeruginosa, Bacillus subtilis and Mucor ramannianus and an activity against Candida albicans.

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