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2-(7-methoxy-1,2,3,4-tetrahydronaphthalen-1-yl)acetohydrazide is a complex organic compound with the molecular formula C13H17NO2. It is a derivative of naphthalene, a bicyclic aromatic hydrocarbon, with a tetrahydro structure, meaning that one of the double bonds in the naphthalene ring has been reduced to a single bond. The compound features a 7-methoxy group, which is a methoxy (-OCH3) group attached to the seventh carbon of the naphthalene ring. Additionally, it contains an acetohydrazide moiety, which is a hydrazide group (-NHNH2) attached to an acetic acid group (-COOH). This chemical is primarily used in the synthesis of various pharmaceuticals and has potential applications in the development of new drugs due to its unique structure and properties.

5454-89-7

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5454-89-7 Usage

Molecular structure

A complex structure with a substituted naphthalene ring system, a methoxy group at the 7-position, and a carbonyl group attached to an acetohydrazide moiety.

Naphthalene ring

A fused ring system consisting of two benzene rings.

Methoxy group

An oxygen atom attached to a methyl group (-OCH3) at the 7-position of the naphthalene ring.

Acetohydrazide moiety

A carbonyl group (C=O) attached to a hydrazide group (-NHNH2).

Pharmaceutical research

Due to its unique structure, it may have potential interactions with biological systems, making it a candidate for further study in drug development.

Reactivity

Further study is needed to understand the reactivity of 2-(7-methoxy-1,2,3,4-tetrahydronaphthalen-1-yl)acetohydrazide, as it may have specific reactivity patterns due to its complex molecular structure.

Characterization

Further characterization of its properties, such as solubility, stability, and spectroscopic data, is necessary to fully understand its implications and potential value.

Research and development

Further study and characterization of 2-(7-methoxy-1,2,3,4-tetrahydronaphthalen-1-yl)acetohydrazide are essential to explore its potential applications and understand its properties better.

Safety and toxicity

Information on the safety and toxicity of 2-(7-methoxy-1,2,3,4-tetrahydronaphthalen-1-yl)acetohydrazide is not provided, and further research is needed to determine its potential hazards and safe handling procedures.

Synthesis

The synthesis method for 2-(7-methoxy-1,2,3,4-tetrahydronaphthalen-1-yl)acetohydrazide is not mentioned in the material provided, but it would be an essential aspect to study for potential large-scale production or pharmaceutical applications.

Structural analogs

Further research could explore the properties and potential applications of structural analogs of 2-(7-methoxy-1,2,3,4-tetrahydronaphthalen-1-yl)acetohydrazide, which may have similar or different properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 5454-89-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5454-89:
(6*5)+(5*4)+(4*5)+(3*4)+(2*8)+(1*9)=107
107 % 10 = 7
So 5454-89-7 is a valid CAS Registry Number.

5454-89-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(7-methoxytetralin-1-yl)acetohydrazide

1.2 Other means of identification

Product number -
Other names 3-Carboxy-7-methoxyquinoline

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:5454-89-7 SDS

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