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N-(4-bromophenyl)-4-oxo-4-phenylbutanamide is a complex organic compound with the molecular formula C15H12BrNO2. It is a derivative of butanamide, featuring a 4-bromophenyl group attached to the nitrogen atom, a phenyl group at the 4-position, and a carbonyl group at the 4-oxo position. N-(4-bromophenyl)-4-oxo-4-phenylbutanamide is characterized by its aromatic structure and the presence of a bromine atom, which may contribute to its reactivity and potential applications in chemical synthesis. It is important to note that the specific properties, such as solubility, stability, and reactivity, can vary depending on the conditions and the context in which the compound is used.

6621-86-9

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6621-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6621-86-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6621-86:
(6*6)+(5*6)+(4*2)+(3*1)+(2*8)+(1*6)=99
99 % 10 = 9
So 6621-86-9 is a valid CAS Registry Number.

6621-86-9SDS

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-(4-bromophenyl)-4-oxo-4-phenylbutanamide

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

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More Details:6621-86-9 SDS

6621-86-9Downstream Products

6621-86-9Relevant academic research and scientific papers

Bromination of 5-substituted 3H-furan-2-ones and 3H-pyrrol-2-ones

Egorova,Sedavkina

, p. 1319 - 1323 (2002)

The bromination of 5-alkyl(aryl)-3H-furan-2-ones and 5-alkyl(aryl)-3H-pyrrol-2-ones and also their derivatives takes place at the ethylene bond with the formation of 4-monobromo derivatives. N-Phenyl-3H-pyrrol-2-ones are brominated simultaneously at the e

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