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1-(9-bromophenanthren-3-yl)-2-(dibutylamino)ethanone is a complex organic compound with the molecular formula C22H28BrNO. It is characterized by a phenanthrene core, which is a tricyclic aromatic hydrocarbon, with a bromine atom at the 9th position. The molecule also features a butylamino group attached to the ethanone (ketone) functional group, which is connected to the phenanthrene through a carbon-carbon single bond. This chemical structure endows the compound with unique electronic and steric properties, making it potentially useful in various chemical and pharmaceutical applications, such as the synthesis of complex organic molecules or as intermediates in the production of pharmaceuticals. The specific reactivity and applications of 1-(9-bromophenanthren-3-yl)-2-(dibutylamino)ethanone would depend on its physical and chemical properties, which are not detailed in this summary.

6338-95-0

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6338-95-0 Usage

Chemical structure

The compound consists of a phenanthrene ring with a bromine atom attached at the 9 position, and an ethanone group attached to a dibutylamino group.

Potential applications

Due to its unique structure and properties, 1-(9-bromophenanthren-3-yl)-2-(dibutylamino)ethanone has the potential to be used in various applications such as pharmaceuticals, dyes, and organic synthesis.

Biological activities

The compound may have potential biological activities that make it of interest for further research and development.

Molecular weight

The molecular weight of the compound is approximately 398.35 g/mol.

Physical state

The compound is likely to be a solid at room temperature, based on its molecular weight and structure.

Solubility

The solubility of 1-(9-bromophenanthren-3-yl)-2-(dibutylamino)ethanone is not explicitly mentioned in the material provided, but it may be soluble in organic solvents such as ethanol, acetone, or dichloromethane.

Stability

The stability of the compound is not explicitly mentioned in the material provided, but it may be sensitive to light, heat, or moisture, as is common with many organic compounds.

Synthesis

The synthesis of 1-(9-bromophenanthren-3-yl)-2-(dibutylamino)ethanone is not described in the material provided, but it likely involves the formation of the phenanthrene ring, bromination at the 9 position, and subsequent reaction with dibutylaminoethyl ketone.

Check Digit Verification of cas no

The CAS Registry Mumber 6338-95-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6338-95:
(6*6)+(5*3)+(4*3)+(3*8)+(2*9)+(1*5)=110
110 % 10 = 0
So 6338-95-0 is a valid CAS Registry Number.

6338-95-0SDS

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 1-(9-bromophenanthren-3-yl)-2-(dibutylamino)ethanone,hydrochloride

1.2 Other means of identification

Product number -
Other names 1-(9-BROMOPHENANTHREN-3-YL)-2-(DIBUTYLAMINO)ETHANONE HYDROCHLORIDE

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:6338-95-0 SDS

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