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3-bromo-4-hydroxynaphthalene-1,2-dione is a chemical compound characterized by the molecular formula C10H5BrO3. It is a derivative of naphthalene, featuring a bromine atom and a hydroxyl group attached to the naphthalene ring. This versatile compound is widely recognized for its potential applications across various industries due to its unique chemical properties.

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  • 1203-39-0 Structure
  • Basic information

    1. Product Name: 3-bromo-4-hydroxynaphthalene-1,2-dione
    2. Synonyms:
    3. CAS NO:1203-39-0
    4. Molecular Formula: C10H5BrO3
    5. Molecular Weight: 253.0489
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1203-39-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 366.6°C at 760 mmHg
    3. Flash Point: 175.5°C
    4. Appearance: N/A
    5. Density: 1.948g/cm3
    6. Vapor Pressure: 5.09E-06mmHg at 25°C
    7. Refractive Index: 1.737
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-bromo-4-hydroxynaphthalene-1,2-dione(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-bromo-4-hydroxynaphthalene-1,2-dione(1203-39-0)
    12. EPA Substance Registry System: 3-bromo-4-hydroxynaphthalene-1,2-dione(1203-39-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1203-39-0(Hazardous Substances Data)

1203-39-0 Usage

Uses

Used in Organic Synthesis:
3-bromo-4-hydroxynaphthalene-1,2-dione serves as a key intermediate in organic synthesis, facilitating the creation of a broad spectrum of chemical products. Its presence in the synthesis process is crucial for the formation of complex organic molecules, which are essential in various applications.
Used in Pharmaceutical Preparation:
In the pharmaceutical industry, 3-bromo-4-hydroxynaphthalene-1,2-dione is utilized as a reagent for the preparation of various drugs. Its unique structure allows it to be a building block in the development of new medicinal compounds, contributing to the advancement of healthcare solutions.
Used in Agrochemical Production:
3-bromo-4-hydroxynaphthalene-1,2-dione also finds application in the agrochemical sector, where it is employed in the production of pesticides and other agricultural chemicals. Its role in this industry is vital for enhancing crop protection and ensuring food security.
Used in Dye and Pigment Manufacturing:
3-bromo-4-hydroxynaphthalene-1,2-dione is further utilized in the manufacturing of dyes and pigments, where its chemical properties contribute to the coloration and stability of these products. This application is particularly relevant in the textile, paint, and printing industries, where vibrant and long-lasting colors are desired.

Check Digit Verification of cas no

The CAS Registry Mumber 1203-39-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,0 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1203-39:
(6*1)+(5*2)+(4*0)+(3*3)+(2*3)+(1*9)=40
40 % 10 = 0
So 1203-39-0 is a valid CAS Registry Number.

1203-39-0SDS

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 3-bromo-4-hydroxynaphthalene-1,2-dione

1.2 Other means of identification

Product number -
Other names 2-bromo-3-hydroxynaphthalene-1,4-dione

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:1203-39-0 SDS

1203-39-0Relevant articles and documents

Ethanolysis of 3-Bromo-4--1,2-naphthoquinone

Dabbene, Viviana G.,Brinon, Margarita C.,Bertorello, Maria M. de

, p. 508 - 509 (2007/10/03)

The ethanolysis of 3-bromo-4--1,2-naphthoquinone (1) under various temperature and light conditions is described.

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