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2-[(5-bromonaphthalen-1-yl)carbonyl]benzoic acid is a complex organic compound characterized by its molecular formula C17H11BrO3. 2-[(5-bromonaphthalen-1-yl)carbonyl]benzoic acid features a benzoic acid group attached to a naphthalene ring, with a bromine atom at the 5-position of the naphthalene. The carbonyl group bridges the benzoic acid and the naphthalene, creating a unique structure. It is a white crystalline solid with potential applications in chemical research and pharmaceutical development, particularly in the synthesis of various organic compounds and as a building block for more complex molecules. Due to its specific functional groups and structural features, it may also be of interest in the study of molecular interactions and properties within the fields of material science and medicinal chemistry.

6324-57-8

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6324-57-8 Usage

Benzoic acid derivative

It is a derivative of benzoic acid This means that the compound is structurally related to benzoic acid, with modifications in its structure, such as the presence of a naphthalene ring and a bromine atom.

Benzene ring

Contains a benzene ring A benzene ring is a hexagonal ring of six carbon atoms connected by alternating single and double bonds, which is a fundamental structure in many organic compounds.

Carboxylic acid group

Has a carboxylic acid group A carboxylic acid group (-COOH) is a functional group consisting of a carbonyl group (C=O) and a hydroxyl group (-OH) bonded to the same carbon atom.

Carbonyl group

Has a carbonyl group A carbonyl group (C=O) is a functional group consisting of a carbon atom double-bonded to an oxygen atom, which is present in 2-[(5-bromonaphthalen-1-yl)carbonyl]benzoic acid.

Naphthalene ring

Features a naphthalene ring A naphthalene ring is a fused ring system consisting of two benzene rings sharing two vertices, which is a common structure in many organic compounds.

Bromine substitution

Substituted with a bromine atom The presence of a bromine atom in the compound can affect its chemical properties, such as reactivity, polarity, and solubility.

Potential applications

May have potential applications in pharmaceuticals, organic synthesis, and material science Although further research and testing are needed, 2-[(5-bromonaphthalen-1-yl)carbonyl]benzoic acid could potentially be used in various fields due to its unique structure and properties.

Further research needed

Requires further research and testing to determine exact properties and potential uses As with many new compounds, the full range of properties and potential applications of 2-[(5-bromonaphthalen-1-yl)carbonyl]benzoic acid is not yet fully understood and requires additional investigation.

Check Digit Verification of cas no

The CAS Registry Mumber 6324-57-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6324-57:
(6*6)+(5*3)+(4*2)+(3*4)+(2*5)+(1*7)=88
88 % 10 = 8
So 6324-57-8 is a valid CAS Registry Number.

6324-57-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(5-bromonaphthalene-1-carbonyl)benzoic acid

1.2 Other means of identification

Product number -
Other names HMS3080M17

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:6324-57-8 SDS

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