Welcome to LookChem.com Sign In|Join Free
  • or
1,4-Bis(chloromethyl)naphthalene, with the molecular formula C12H10Cl2, is a chemical compound derived from naphthalene. It is characterized by the presence of two chloromethyl groups attached to the 1,4-positions of the naphthalene ring. 1,4-BISCHLOROMETHYL-NAPHTHALENE serves as a versatile building block in organic synthesis, offering a range of applications across different industries.

6586-89-6

Post Buying Request

6586-89-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

6586-89-6 Usage

Uses

Used in Polymer and Resin Production:
1,4-Bis(chloromethyl)naphthalene is used as a key component in the production of polymers and resins. Its unique structure allows for the formation of strong chemical bonds, contributing to the overall strength and stability of the resulting materials. This makes it suitable for use in various applications, such as coatings, adhesives, and composite materials.
Used in Rubber Manufacturing:
In the rubber industry, 1,4-bis(chloromethyl)naphthalene functions as a cross-linking agent. It helps to create a network of chemical bonds between rubber molecules, enhancing the elasticity, durability, and resistance to wear and tear of the final product. This is particularly important in the manufacturing of tires, hoses, and other rubber-based items that require high performance and longevity.
Used as a Pesticide:
1,4-Bis(chloromethyl)naphthalene is also employed as a pesticide, leveraging its chemical properties to control and eliminate pests in agricultural settings. Its effectiveness in this application is attributed to its ability to disrupt the normal functioning of pests, thereby preventing damage to crops and ensuring a healthy yield.
Used as a Chemical Intermediate in Pharmaceutical Synthesis:
1,4-BISCHLOROMETHYL-NAPHTHALENE serves as a valuable intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with specific therapeutic properties, contributing to advancements in medicine and healthcare.
Used as a Chemical Intermediate in Dye Synthesis:
In the dye industry, 1,4-bis(chloromethyl)naphthalene is utilized as a chemical intermediate for the production of dyes with specific color characteristics and properties. Its involvement in the synthesis process enables the creation of dyes with improved stability, colorfastness, and application versatility.

Check Digit Verification of cas no

The CAS Registry Mumber 6586-89-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,8 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6586-89:
(6*6)+(5*5)+(4*8)+(3*6)+(2*8)+(1*9)=136
136 % 10 = 6
So 6586-89-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H10Cl2/c13-7-9-5-6-10(8-14)12-4-2-1-3-11(9)12/h1-6H,7-8H2

6586-89-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-bis(chloromethyl)naphthalene

1.2 Other means of identification

Product number -
Other names NAPHTHALENE,1,4-BIS(CHLOROMETHYL)

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:6586-89-6 SDS

6586-89-6Relevant academic research and scientific papers

Synthesis and Stability of Aryl Bis(nitrile oxides) with Potential as Curing Agents for Polysulfide Sealants

Hanhela, Peter J.,Paul, D. Brenton

, p. 287 - 299 (2007/10/02)

Several aromatic bis(nitrile oxides) have been prepared as potential curing agents for sealants produced from thiol-terminated polysulfide liquid polymers.All were obtained by dehydrohalogenation of α-halo oximes and the requisite aldehydes were synthesized from either the dimethyl derivatives or the chloromethylated hydrocarbons.The direct chloromethylation of naphthalene which offered a convenient route to the naphthalene-1,4- and 1,5-bis(carbonitrile oxides) was re-examined.Also prepared were naphthalene-2,6-bis(carbonitrile oxide), anthracene-9,10-bis(carbonitrile oxide) and 4,4'-sulfonylbisbenzonitrile dioxide.The course of the reaction between naphthalene-2,3-dicarbaldehyde and hydroxylamine was established and shown to differ from that involving phthalaldehyde.Stabilities of the nitrile oxides at -15 deg C, 4 deg C and 25 deg C were assessed by spectroscopic means.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 6586-89-6