2-amino-3-chloro-1,4- naphthaquinone

CAS Number: 2797-51-5

Molecular Formula: C10H6ClNO2

Purity: 2-amino-3-chloro-1,4-naphthaquinone 98% purity

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About 2-amino-3-chloro-1,4- naphthaquinone

2-Amino-3-chloro-1,4-naphthoquinone (CAS 2797-51-5) serves as a critical high purity fine chemical within the API intermediates market, primarily utilized for the synthesis of advanced antitumor agents and MEK1 inhibitors where a Pharma/API purity 99% or General Industry purity 98% is necessary to ensure precise metabo...

2-amino-3-chloro-1,4- naphthaquinone Specifications

CAS Number

2797-51-5

Molecular Formula

C10H6ClNO2

Molecular Weight

207.61 g/mol

IUPAC Name

2-amino-3-chloronaphthalene-1,4-dione

Canonical SMILES

NC1=C(Cl)C(=O)c2ccccc2C1=O

InChI Key

OBLNWSCLAYSJJR-UHFFFAOYSA-N

HSN No

29223990

CAS Number

2797-51-5

Molecular Formula

C10H6ClNO2

Molecular Weight

207.61 g/mol

IUPAC Name

2-amino-3-chloronaphthalene-1,4-dione

Canonical SMILES

NC1=C(Cl)C(=O)c2ccccc2C1=O

InChI Key

OBLNWSCLAYSJJR-UHFFFAOYSA-N

HSN No

29223990

Molecular Weight

207.61 g/mol

Purity

2-amino-3-chloro-1,4-naphthaquinone 98% purity

Physical appearance

Orange to amber to dark red powder to crystal

Melting Point

198-203 °C

Boiling Point

310℃

Freezing point

199-203°C

Flash Point

141 °C

logP

1.52

Precautionary Statement Codes

P203, P260, P261, P264, P264+P265, P270, P272, P273, P280, P301+P317, P302+P352, P305+P351+P338, P318, P319, P321, P330, P333+P317, P337+P317, P362+P364, P391, P405, and P501

Hazard Classes and Categories

Acute Tox. 4 (100%) Skin Sens. 1 (18.8%)

Agrochemical Intermediate

A critical active ingredient and precursor used primarily as a herbicide (quinoclamine) for weed and algae management in agricultural and environmental applications

Pharmaceutical Intermediate

A versatile building block utilized in the synthesis of bioactive compounds, particularly in the development of anti-cancer, antibacterial, and antimalarial agents

Dye and Pigment Intermediate

A functionalized naphthoquinone used in the production of stable, light-resistant dyes and organic pigments for textiles and inks

Research Reagent

A valuable tool in biochemical assays and electrochemical sensor development due to its unique redox properties and reactivity in oxidative stress studies.