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2-(7-methylnaphthalen-1-yl)ethyl 4-nitrobenzoate is a complex organic compound with the molecular formula C19H17NO4. It is characterized by a naphthalene ring with a methyl group at the 7th position, an ethyl group attached to the 2nd position of the naphthalene, and a 4-nitrobenzoate group esterified to the ethyl group. 2-(7-methylnaphthalen-1-yl)ethyl 4-nitrobenzoate is known for its potential applications in the synthesis of various pharmaceuticals and chemical intermediates due to its unique structure and reactivity. It is typically synthesized through a series of chemical reactions involving naphthalene derivatives and nitrobenzoic acid, and its properties, such as solubility and stability, are influenced by the presence of the nitro group and the aromatic rings. The compound is an example of the vast array of organic molecules that can be created through chemical synthesis, showcasing the diversity and complexity of organic chemistry.

7501-42-0

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7501-42-0 Usage

7-methylnaphthalene moiety

A naphthalene ring structure with a methyl group attached to the seventh carbon atom. This group is a part of the compound's structure and contributes to its chemical properties.

Ethyl group

A two-carbon chain with a hydrogen atom and a methyl group attached to each carbon. The ethyl group connects the 7-methylnaphthalene moiety to the 4-nitrobenzoate group.

4-nitrobenzoate group

A benzene ring with a nitro group (-NO2) attached to the fourth carbon atom and a carboxylate group (-COO-) attached to the first carbon atom. This group is responsible for the compound's acidic properties and contributes to its reactivity.

Building block for organic synthesis

The compound can be used as a starting material for the preparation of other organic compounds through chemical reactions.

Research applications

The compound may be used in academic or industrial research to study its chemical properties and potential applications.

Potential pharmaceutical applications

The compound may have potential uses in the pharmaceutical industry due to its structural features and potential pharmacological activities.

Context-dependent properties and applications

The specific properties and applications of the compound would depend on the context in which it is used, such as the desired chemical reaction or the target medical condition.

Check Digit Verification of cas no

The CAS Registry Mumber 7501-42-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,0 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7501-42:
(6*7)+(5*5)+(4*0)+(3*1)+(2*4)+(1*2)=80
80 % 10 = 0
So 7501-42-0 is a valid CAS Registry Number.

7501-42-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(7-methylnaphthalen-1-yl)ethyl 4-nitrobenzoate

1.2 Other means of identification

Product number -
Other names 1-(7-Methyl-[1]naphthyl)-2-(4-nitro-benzoyloxy)-aethan

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:7501-42-0 SDS

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