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70373-49-8

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  • 2-Cyano-N-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)acetamide

    Cas No: 70373-49-8

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70373-49-8 Usage

General Description

2-CYANO-N-(1,5-DIMETHYL-3-OXO-2-PHENYL-2,3-DIHYDRO-1H-PYRAZOL-4-YL)-ACETAMIDE is a chemical compound with the molecular formula C16H18N4O2. It is an acetyl amide derivative with the substituent 2-cyano-n-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1h-pyrazol-4-yl)-acetamide. 2-CYANO-N-(1,5-DIMETHYL-3-OXO-2-PHENYL-2,3-DIHYDRO-1H-PYRAZOL-4-YL)-ACETAMIDE has potential biological activity and may be used in medicinal and pharmaceutical research. Its specific properties and potential uses may vary depending on the context and combination with other compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 70373-49-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,3,7 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 70373-49:
(7*7)+(6*0)+(5*3)+(4*7)+(3*3)+(2*4)+(1*9)=118
118 % 10 = 8
So 70373-49-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H14N4O2/c1-10-13(16-12(19)8-9-15)14(20)18(17(10)2)11-6-4-3-5-7-11/h3-7H,8H2,1-2H3,(H,16,19)

70373-49-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-cyano-N-(1,5-dimethyl-3-oxo-2-phenylpyrazol-4-yl)acetamide

1.2 Other means of identification

Product number -
Other names 4-cyano acetamidophenazone

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:70373-49-8 SDS

70373-49-8Relevant articles and documents

Synthesis, Antimicrobial Activity and Molecular Modeling of Some Novel 5-Aminopyrazole, Pyrazolo[1,5-a]pyrimidine, Bispyrazole and Bispyridone Derivatives Containing Antipyrinyl Moiety

Helal, Mohamed Hamdy,Salem, Mohamed A.,Aly, Hala Mohamed

, p. 2614 - 2626 (2017)

2-Cyano-N-(antipyrin-4-yl)-3-(ethylthio)-3-(naphthalen-1-ylamino)acryl-amide 4 was achieved via a one-pot, three-component reactions of cyanoacetamide derivative 2, 2-naphthyl isothiocyanate, and diethyl-sulphate. The cyano acrylamide derivative 4 was hydrazinolysis to furnish 5-aminopyrazole 5; many pyrazolo[1,5-a]pyrimidines 10a,b, 14, 15, 16, 18, and 20 have been synthesized via treatment of 5 with some electrophilic reagents. Also, ternary condensation of cyanoacetamide derivative 2, terephthalaldehyde, and active methylene derivatives afforded bispyridone derivatives 21a,b. The structures of the new compounds were confirmed on the basis of elemental analysis and spectral data. Representative compounds of the synthesized products were tested and evaluated as antimicrobial. In general, the novel-synthesized compounds showed a good antimicrobial activity against Gram-positive bacteria, Gram-negative bacteria, and antifungal activity against Azithromycin and Ketoconazole. The molecular modeling of the 21a and 21b as representative examples of the synthesized compounds has been drawn, and their molecular parameters were calculated.

Design and synthesis of some thiazolyl and thiadiazolyl derivatives of antipyrine as potential non-acidic anti-inflammatory, analgesic and antimicrobial agents

Rostom, Sherif A.F.,El-Ashmawy, Ibrahim M.,Abd El Razik, Heba A.,Badr, Mona H.,Ashour, Hayam M.A.

scheme or table, p. 882 - 895 (2009/08/15)

The synthesis of two groups of structure hybrids comprising basically the antipyrine moiety attached to either polysubstituted thiazole or 2,5-disubstituted-1,3,4-thiadiazole counterparts through various linkages is described. Twelve out of the newly synt

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