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76145-96-5

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76145-96-5 Usage

Chemical structure

Ketone derivative with a bromine atom and a biphenyl group attached to a butanone backbone

Explanation

The compound is derived from a ketone, which is a carbonyl compound with a C=O double bond. It has a bromine atom and a biphenyl group (two connected phenyl rings) attached to the carbonyl carbon, and a butanone backbone (a four-carbon chain with a carbonyl group at the end).

Explanation

The compound contains a carbonyl group (C=O) as a ketone, a bromine atom as a halogen, and a biphenyl group as an aromatic system.

Explanation

The compound is used in various fields due to its unique structure and properties. It is particularly useful in the synthesis of pharmaceuticals and agrochemicals, as well as a reagent in chemical reactions. Additionally, it has potential applications in materials science for the creation of functional polymers and other advanced materials.

Explanation

The compound's molecular weight and structure suggest that it is likely to be a solid at room temperature, although specific melting and boiling points are not provided.

Explanation

Due to its nonpolar nature and the presence of a bromine atom, the compound is expected to be soluble in organic solvents such as dichloromethane, ethyl acetate, or acetone.

Explanation

The compound is generally stable under normal conditions, such as room temperature and pressure. However, it may be sensitive to heat, light, or moisture, which could lead to degradation or unwanted reactions.

Explanation

As a chemical compound, 1-(biphenyl-4-yl)-2-bromobutan-1-one may pose health risks if not handled properly. It could be an irritant, toxic, or harmful if it comes into contact with the skin, is inhaled, or is ingested. Proper safety measures and personal protective equipment should be used when working with this compound.

Functional groups

Ketone, bromine, and biphenyl

Applications

Organic synthesis, pharmaceuticals, agrochemicals, reagent in chemical reactions, materials science, functional polymers, and advanced materials

Physical state

Likely a solid at room temperature

Solubility

Soluble in organic solvents

Stability

Stable under normal conditions

Hazards

Potential irritant, toxic, or harmful if ingested, inhaled, or absorbed through the skin

Check Digit Verification of cas no

The CAS Registry Mumber 76145-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,1,4 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 76145-96:
(7*7)+(6*6)+(5*1)+(4*4)+(3*5)+(2*9)+(1*6)=145
145 % 10 = 5
So 76145-96-5 is a valid CAS Registry Number.

76145-96-5SDS

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 2-bromo-1-(4-phenylphenyl)butan-1-one

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:76145-96-5 SDS

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