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4-ethyl-N-(2-{[1-(4-fluorophenyl)-3-phenyl-1H-pyrazol-5-yl]amino}-2-oxoethyl)-N-(1-methylethyl)benzamide is a complex organic compound with a molecular formula of C30H28FN3O3. It is a derivative of benzamide, featuring a 4-ethylbenzamide core with a substituted pyrazole ring and an additional 2-oxoethyl group. The pyrazole ring is adorned with a 4-fluorophenyl and a phenyl group, while the 2-oxoethyl group is connected to an isopropylamine moiety. This chemical structure suggests potential applications in medicinal chemistry, possibly as a precursor or an intermediate in the synthesis of pharmaceuticals, given the presence of a benzamide scaffold and a pyrazole ring, which are common in various bioactive molecules. However, without specific context or application, it is challenging to provide a detailed summary of its properties or uses.

5881-62-9

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5881-62-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5881-62-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,8 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5881-62:
(6*5)+(5*8)+(4*8)+(3*1)+(2*6)+(1*2)=119
119 % 10 = 9
So 5881-62-9 is a valid CAS Registry Number.

5881-62-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethyl-N-[2-[[2-(4-fluorophenyl)-5-phenylpyrazol-3-yl]amino]-2-oxoethyl]-N-propan-2-ylbenzamide

1.2 Other means of identification

Product number -
Other names 2,5-Dimethyl-4-(3-nitrophenyl)-3-pyrrolcarbonsaeure-ethylester

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:5881-62-9 SDS

5881-62-9Downstream Products

5881-62-9Relevant academic research and scientific papers

Heterocycles from α-Nitroolefins, VIII. - 2-Methyl-3-pyrrolecarboxylates from α-Nitroolefins and Acetoacetates

Boberg, Friedrich,Garburg, Karl-Heinz,Goerlich, Karl-Joachim,Pipereit, Eberhard,Ruhr, Maria

, p. 239 - 250 (2007/10/02)

3-Pyrrolecarboxylates 4 can be prepared from α-nitroolefins 1 and acetoacetates 2 by two methods: (a) 1 and 2 react to give 4,5-dihydro-5-methyleneamino-3-furancarboxylates 3 which are hydrolyzed, (b) the nitronic acids 8, adducts of 1 and 2, yield with different reduction agents the heterocycles 4.

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