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4-Chloro-2,6-bis(chloromethyl)phenol is an organic compound with the chemical formula C8H7Cl3O. It is a derivative of phenol, featuring a chlorine atom at the 4-position and two chloromethyl groups attached to the 2 and 6 positions of the benzene ring. This white crystalline solid is soluble in organic solvents and has a molecular weight of 233.50 g/mol. The compound is primarily used as an intermediate in the synthesis of various chemicals, including pharmaceuticals and agrochemicals. Due to its reactive nature and potential health hazards, it is important to handle this chemical with proper safety measures.

6641-03-8

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6641-03-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6641-03-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,4 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6641-03:
(6*6)+(5*6)+(4*4)+(3*1)+(2*0)+(1*3)=88
88 % 10 = 8
So 6641-03-8 is a valid CAS Registry Number.

6641-03-8SDS

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 4-chloro-2,6-bis(chloromethyl)phenol

1.2 Other means of identification

Product number -
Other names 5-Chlor-2-hydroxy-1.3-bis-chlormethyl-benzol

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:6641-03-8 SDS

6641-03-8Relevant academic research and scientific papers

Magnetic and structural properties of dinuclear singly bridged-phenoxido metal(II) complexes

Massoud, Salah S.,Spell, Mark,Ledet, Catherine C.,Junk, Thomas,Herchel, Radovan,Fischer, Roland C.,Trvnek, Zdenk,Mautner, Franz A.

, p. 2110 - 2121 (2015/01/30)

The reaction of a methanolic solution containing the bi-compartmental phenolic ligand 2,6-bis[bis(2-pyridylmethyl)aminomethyl]-4-chlorophenol (LCl-OH) with MCl2·nH2O in the presence of NH4PF6 or NaClO4 afforded the dinuclear bridged-phenoxido dichlorido-metal(ii) complexes [Co2(μ-LClO)(H2O)2Cl2][Co2(μ-LClO)(MeOH)2Cl2](PF6)2 (1), [Ni2(μ-LClO)(MeOH)2Cl2]PF6 (2), [Ni2(μ-LClO)(MeOH)(H2O)Cl2]ClO4·1.25H2O (3), [Cu2(μ-LClO)Cl2]PF6·1/2MeOH (4) and [Zn2(μ-LClO)Cl2]PF6·MeOH (5). The complexes were characterized by elemental microanalyses, conductivity measurements, IR and UV-Vis spectroscopy, mass spectrometry and single crystal X-ray crystallography. Each M(ii) center within the dinuclear complex cations is octahedrally coordinated in complexes 1-3, and five-coordinated distorted square pyramidal in 4 and 5. Magnetic susceptibility measurements at variable temperature of the complexes 1-4 revealed weak to moderate antiferromagnetic coupling with |J| values = 8.38, 39.0, 30.2 and 0.79 cm-1, respectively. The results of DFT calculations correlate well with the experimentally determined antiferromagnetic coupling and show that the magnetic exchange coupling occurs mainly through the phenoxido bridge M-O-M. Implications of geometry around the central metal ion, M...M distance, M-O-M bond angle and overlapping of magnetic orbitals on the magnetic exchange coupling are discussed.

Treatment of animals with 2,6-bis(2-hydroxybenzyl)phenols to eradicate trematodes

-

, (2008/06/13)

A process for killing internal parasites of warm blooded animals which process comprises treating the infected animal with an effective amount of a composition comprising as active ingredient a compound of the general formula I: STR1 wherein R1

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