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1-Hexadecanone, 1-[4-(bromomethyl)phenyl]- is an organic compound with the molecular formula C23H37BrO. It is a derivative of hexadecanone, featuring a bromomethyl group attached to a phenyl ring at the 4-position. This chemical is characterized by a long aliphatic chain (hexadecane) with a ketone group at one end and a substituted phenyl ring at the other. The presence of the bromine atom in the molecule makes it a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its unique structure, it exhibits properties such as low solubility in water and high solubility in organic solvents. It is also known for its potential applications in the field of materials science, particularly in the development of new polymers and coatings.

2551-16-8

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2551-16-8 Usage

Chemical Class

Ketones

Explanation

1-Hexadecanone, 1-[4-(bromomethyl)phenyl]belongs to the class of ketones, which are organic compounds with a carbonyl group (C=O) bonded to two other carbon atoms.

Explanation

The compound appears as a white to light yellow solid at room temperature.

Explanation

1-Hexadecanone, 1-[4-(bromomethyl)phenyl]is used in the production of flavors and fragrances, as well as in the synthesis of pharmaceuticals and other organic compounds due to its unique chemical properties.

Explanation

The compound is known to have a strong odor, which can be detected at low concentrations.

Explanation

Inhalation or ingestion of 1-Hexadecanone, 1-[4-(bromomethyl)phenyl]can lead to toxic effects, although the level of toxicity is considered to be slight.

Explanation

Due to its chemical properties and potential effects on the environment, 1-Hexadecanone, 1-[4-(bromomethyl)phenyl]is considered a potential environmental hazard and should be handled with caution.

Explanation

Given its potential toxicity and environmental hazard, it is important to handle 1-Hexadecanone, 1-[4-(bromomethyl)phenyl]with care, using appropriate safety measures and equipment to minimize risks.

Physical State

White to light yellow solid

Applications

Flavors and fragrances, pharmaceuticals, and organic compounds synthesis

Odor

Strong

Toxicity

Slightly toxic when inhaled or ingested

Environmental Hazard

Potential environmental hazard

Handling Precautions

Handle with care

Check Digit Verification of cas no

The CAS Registry Mumber 2551-16-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,5 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2551-16:
(6*2)+(5*5)+(4*5)+(3*1)+(2*1)+(1*6)=68
68 % 10 = 8
So 2551-16-8 is a valid CAS Registry Number.

2551-16-8Relevant academic research and scientific papers

SYNTHESE ET ETUDE DE LA DEGRADATION PHOTOCHIMIQUE DE TENSIO-ACTIFS CATIONIQUES PHOTOCLIVABLES

Strub-Leconte, M. P.,Riess, G.

, p. 137 - 144 (2007/10/02)

A homologous series of photocleavable cationic surfactants was prepared.These aryl-alkyl-ketone type surfactants have the following structure .Their critical micelle concentration in water was determined.The photodegradation study has shown that the cleavage occurs with a high quantum yield by a Norrish II mechanism with formation of alkene, substituted acetophenone and cyclobutanols.The photochemical yield of cleavage reaches 75 percent with formation of a hydrophilic (substituted acetophenone) and a hydrophobic derivative (alkene).

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