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1-Bromo-2-chloronaphthalene, with the molecular formula C10H6BrCl, is a halogenated derivative of naphthalene, an aromatic hydrocarbon. It is a colorless to pale yellow liquid characterized by a strong, aromatic odor. As a chemical compound, it is recognized for its role as a building block in the synthesis of a variety of organic compounds, including dyes, pharmaceuticals, and pesticides. Additionally, it serves as a solvent and a chemical intermediate in the production of other chemicals. Due to its potential hazards to human health and the environment, it necessitates careful handling and storage.

71436-66-3

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71436-66-3 Usage

Uses

Used in Chemical Synthesis:
1-Bromo-2-chloronaphthalene is used as a building block for the synthesis of various organic compounds, such as dyes, pharmaceuticals, and pesticides. Its unique halogenated structure allows for versatile chemical reactions, making it a valuable component in the creation of a wide range of products.
Used in Solvent Applications:
As a solvent, 1-Bromo-2-chloronaphthalene is utilized in various industrial processes due to its ability to dissolve other substances. Its solvent properties are particularly useful in the chemical industry for facilitating reactions and aiding in the production of different compounds.
Used in Chemical Intermediates:
1-Bromo-2-chloronaphthalene also serves as a chemical intermediate, playing a crucial role in the production of other chemicals. Its intermediate status allows it to be transformed into a variety of end products, contributing to the versatility and utility of 1-Bromo-2-chloronaphthalene in the chemical manufacturing sector.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-Bromo-2-chloronaphthalene is used as a key component in the development of new drugs. Its unique chemical properties make it suitable for the synthesis of pharmaceutical compounds that can address various medical needs.
Used in Pesticide Production:
1-Bromo-2-chloronaphthalene is employed in the production of pesticides, where it contributes to the creation of effective and targeted pest control agents. Its role in this industry is vital for the development of agricultural chemicals that protect crops and enhance food security.
Used in Dye Manufacturing:
In the dye manufacturing industry, 1-Bromo-2-chloronaphthalene is used as a starting material for the synthesis of various dyes. Its chemical structure allows for the production of dyes with specific color properties, making it an essential component in the creation of a diverse range of dyes for different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 71436-66-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,4,3 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 71436-66:
(7*7)+(6*1)+(5*4)+(4*3)+(3*6)+(2*6)+(1*6)=123
123 % 10 = 3
So 71436-66-3 is a valid CAS Registry Number.

71436-66-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-2-chloronaphthalene

1.2 Other means of identification

Product number -
Other names 1-Brom-2-chlor-naphthalin

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:71436-66-3 SDS

71436-66-3Relevant academic research and scientific papers

Generation of 2-Chloronaphthalene-1,3-diyl

Billups, W.E.,Buynak, John D.,Butler, Dorothy

, p. 4636 - 4641 (2007/10/02)

Reaction of 1-bromo-3,4-benzo-6,6-dichlorobicyclohexane with potassium tert-butoxide in tetrahydrofuran yields 2-chloronaphthalene along with nine other naphthalenes which result from solvent incorporation or reaction with nucleophile (Br-, Cl-, t-BuO-).Use of tetrahydrofuran-d8 as the solvent leads to the incorporation of two deuterium atoms into the chloronaphthalene.This result is interpreted in terms of a 1,3-dehydronaphthalene opening to the diradical, followed by abstraction of deuterium atoms from the solvent.The products which result from incorporation of solvent would then arise by dimerization of radical pairs.The remaining products are thought to arise from nucleophilic addition to the closed form of the dehydronaphthalene.

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