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

104373-97-9

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104373-97-9 Usage

Chemical Class

Acrylamides

Physical State

White solid

Melting Point

148-150°C

Solubility

Sparingly soluble in water

Industrial Applications

Intermediate for the synthesis of pharmaceuticals, dyes, and other organic compounds
Building block for polymer production
Reagent in organic synthesis

Biological Activities

Studied for anti-cancer properties
Investigated for anti-inflammatory properties

Safety Concerns

Classified as a hazardous substance
Can cause irritation to the skin, eyes, and respiratory system upon exposure

Check Digit Verification of cas no

The CAS Registry Mumber 104373-97-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,3,7 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 104373-97:
(8*1)+(7*0)+(6*4)+(5*3)+(4*7)+(3*3)+(2*9)+(1*7)=109
109 % 10 = 9
So 104373-97-9 is a valid CAS Registry Number.

104373-97-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3-acetylphenyl)prop-2-enamide

1.2 Other means of identification

Product number -
Other names -

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:104373-97-9 SDS

104373-97-9Relevant academic research and scientific papers

Synthesis of 4-Trifluoromethylated 1,3-Butadienes via Palladium Catalyzed Heck Reaction

Li, Yang,Hao, Meng,Chang, Yu-Chen,Liu, Yuan,Wang, Wen-Fei,Sun, Ning,Zhu, Wen-Qing,Gao, Ziwei

supporting information, p. 2962 - 2966 (2021/08/23)

1,3-Butadiene plays a key role in modern synthetic chemistry and biochemistry because it is a key intermediate in the synthesis of many drugs. A new and effective method for the synthesis of 4-trifluoromethylated 1,3-butadiene through the fluorinated Heck reaction catalyzed by Pd(0) is described. Without additives, 1-chloro-3,3,3-trifluoropropene (an inexpensive CF3 structural unit that is harmless to ozone) reacts with enamide to synthesize 4-trifluoromethylated 1,3-butadienes with good yield, high regioselectivity and chemical selectivity, and strong tolerance of substrate functional groups such as alkynes, aldehyde, and ester groups.

1-(2-Pyridinyl)piperazine Derivatives with Antianaphylactic, Antibronchospastic, and Mast Cell Stabilizing Activities

Catto, Alberto,Motta, Gianni,Tajana, Alberto,Cazzulani, Pietro,Nardi, Dante,Leonardi, Amedeo

, p. 13 - 19 (2007/10/02)

New 1-(2-pyridinyl)piperazine derivatives were synthesized and tested as inhibitors of the reaginic passive cutaneous anaphylaxis in the rat (PCA), of the histamine-induced bronchospasm in the guinea pig, and of the rat mesenteric mast cell degranulation induced by compound 48/80.On the basis of test results, a series of N-(substituted phenyl)-ω-alkanamides were prepared.The nature of substituents at the anilide ring strongly influenced mast cell stabilizing activity, whereas it was less determining in the case of the other two tests.No clear correlation between the most common physicochemical parameters (?, ?, Vw volume) of substituents and activity could be detected.With regard to the position of substituents at the anilide ring, the rank order of potency, in the PCA and bronchoconstriction tests, was para > meta > ortho.Introduction of substituents in the 1-(2-pyridinyl)piperazinyl moiety of the N-(substituted phenyl)propanamide derivatives hardly affected activity, or the effect was deleterious.Some of the new compounds exhibited a simultaneous remarkable activity in all the three assays employed.

Synthesis of Benzoquinolizine Derivatives

Merchant, J. R.,Pathare, P. M.

, p. 471 - 472 (2007/10/02)

The reaction of α,β-unsaturated acids with aromatic amines in the presence of PPA affords directly benzo-quinolizines (I).The structures of all the compounds have been established on the basis of elemental analyses and spectral data.

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