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N-(2-Naphthalenyl)-3-phenylpropenamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55255-54-4

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55255-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55255-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,5 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55255-54:
(7*5)+(6*5)+(5*2)+(4*5)+(3*5)+(2*5)+(1*4)=124
124 % 10 = 4
So 55255-54-4 is a valid CAS Registry Number.
InChI:InChI=1/C19H15NO/c21-19(13-10-15-6-2-1-3-7-15)20-18-12-11-16-8-4-5-9-17(16)14-18/h1-14H,(H,20,21)

55255-54-4SDS

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 (E)-N-naphthalen-2-yl-3-phenylprop-2-enamide

1.2 Other means of identification

Product number -
Other names Zimtsaeure-<naphthyl-(2)-amid>

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:55255-54-4 SDS

55255-54-4Downstream Products

55255-54-4Relevant academic research and scientific papers

Synthesis and anti-inflammatory activity of 1-acetyl-5-substitute daryl-3-(β-aminonaphthyl)-2-pyrazolines and β-(substitute daminoethyl) amidonaphthalenes

Bansal, Ekta,Srivastava,Kumar, Ashok

, p. 81 - 92 (2007/10/03)

The title compounds were prepared by reaction of β-acetylamino-naphthalene with different aromatic aldehydes followed by cyclisation with hydrazine hydrate and with different primary or secondary amines (Mannich's reaction), respectively. The structures of new compounds were confirmed by 1H-NMR and IR spectral data. Anti-inflammatory and ulcerogenic activities in vivo were evaluated and compared with the standard drugs, phenylbutazone and indomethacin. Some compounds of the series exhibited promising anti-inflammatory activity with a lower ulcerogenic liability than the standard drugs.

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