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Ethyl 1-{4-oxo-5-[(1-phenyl-3-pyridin-4-yl-1H-pyrazol-4-yl)methylidene]-4,5-dihydro-1,3-thiazol-2-yl}piperidine-4-carboxylate is a complex organic compound with a molecular formula of C28H26N4O3S. It is characterized by a 1,3-thiazole ring, which is fused to a 4,5-dihydro-1H-pyrazole ring. The molecule features a piperidine-4-carboxylate group and a phenyl-pyridinyl-pyrazol-4-ylmethylidene moiety, which contributes to its unique structure. ethyl 1-{4-oxo-5-[(1-phenyl-3-pyridin-4-yl-1H-pyrazol-4-yl)methylidene]-4,5-dihydro-1,3-thiazol-2-yl}piperidine-4-carboxylate is of interest in medicinal chemistry due to its potential biological activities and is often studied for its interactions with various biological targets, such as enzymes or receptors, which could lead to the development of new therapeutic agents.

7061-41-8

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7061-41-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7061-41-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,6 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7061-41:
(6*7)+(5*0)+(4*6)+(3*1)+(2*4)+(1*1)=78
78 % 10 = 8
So 7061-41-8 is a valid CAS Registry Number.

7061-41-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1-[4-oxo-5-[(1-phenyl-3-pyridin-4-ylpyrazol-4-yl)methylidene]-1,3-thiazol-2-yl]piperidine-4-carboxylate

1.2 Other means of identification

Product number -
Other names 1,2-bis(4-nitrophenyl)-1,1,2,2-tetracyanoethane

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:7061-41-8 SDS

7061-41-8Downstream Products

7061-41-8Relevant academic research and scientific papers

Anomalous Reaction of Arylmalononitriles with Nitric Acid. Para-Directing Nature of Dicyanomethyl Group and a Through-Ring Nitro/aci-Nitro Tautomerism of 4-Nitrophenylmalononitrile

Suzuki, Hitomi,Koide, Hideki,Ogawa, Takuji

, p. 501 - 504 (2007/10/02)

Phenylmalononitrile reacts with nitric acid in dichloromethane at room temperature to afford 1,2-bis(4-nitrophenyl)-1,1,2,2-tetracyanoethane as an initial product, which readily suffers oxidative cleavage to give 4-nitrobenzoyl cyanide.Contrary to common

CARBON-CARBON BOND FORMATION BY COORDINATION OF CARBOCATIONS WITH CARBANIONS.

Arnett, Edward M.,Troughton, E. B.

, p. 3299 - 3302 (2007/10/02)

Direct attack of resonance-stabilized carbenium ions and carbanions can be regulated to provide a wide range of rates and equilibria for the study of carbon-carbon bond formation.

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