5862-32-8

Basic information

• Product Name: 2,6-BIS(CHLOROMETHYL)-4-METHYLPHENOL, 97
• Synonyms: 2,6-BIS(CHLOROMETHYL)-4-METHYLPHENOL, 97;alpha(sup2),alpha(sup6)-dichloro-mesito;2-Hydroxy-5-methyl-1,3-xylylene dichloride;2,6-Bis(chloromethyl)-4-methylphenol 97%
• CAS NO: 5862-32-8
• Molecular Formula: C₉H₁₀Cl₂O
• Molecular Weight: 205.08
• Product Categories: Building Blocks;C9 to C20+;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds;Phenols
• Mol File: 5862-32-8.mol
• Article Data: 15

Chemical Properties

• Melting Point: 76-83 °C
• Boiling Point: 314.4°Cat760mmHg
• Flash Point: 127.3°C
• Appearance: /
• Density: 1.285g/cm³
• Vapor Pressure: 0.000254mmHg at 25°C
• Refractive Index: 1.571
• PKA: 9.04±0.50(Predicted)
• CAS DataBase Reference: 2,6-BIS(CHLOROMETHYL)-4-METHYLPHENOL, 97(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-BIS(CHLOROMETHYL)-4-METHYLPHENOL, 97(5862-32-8)
• EPA Substance Registry System: 2,6-BIS(CHLOROMETHYL)-4-METHYLPHENOL, 97(5862-32-8)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• RIDADR: UN 3335
• WGK Germany: 3
• RTECS: OX6600000
• Hazardous Substances Data: 5862-32-8(Hazardous Substances Data)

Usage

General Description

"2,6-BIS(CHLOROMETHYL)-4-METHYLPHENOL, 97" is a chemical compound that contains two chloromethyl groups and a methyl group attached to a phenol ring. It is commonly used as a disinfectant, sanitizer, and preservative in various industrial and commercial applications. The compound has a purity level of 97% and is known for its strong antimicrobial and antifungal properties. It is often added to products such as soaps, detergents, and sanitizing solutions to help prevent the growth of bacteria and mold. Additionally, it can also be used as a chemical intermediate in the production of other compounds.

InChI:InChI=1/C9H10Cl2O/c1-6-2-7(4-10)9(12)8(3-6)5-11/h2-3,12H,4-5H2,1H3

Upstream product

• 91-04-3 2,6-bis(hydroxymethyl)-4-methylphenol 
• 7647-01-0 hydrogenchloride 
• 409317-20-0 2-hydroxy-5-methyl-3-thiocyanatomethyl-benzyl alcohol 
• 71-43-2 benzene 
• 106-44-5 p-cresol 

Downstream Products

• 1620-68-4 2,6-bis(2-hydroxy-5-methylbenzyl)-4-methylphenol 
• 66232-87-9 GRI 406402 
• 55036-44-7 2,2',2,2'-(((2-hydroxy-5-methyl-1,3-phenylene)bis(methylene))bis(azanetriyl))tetraacetic acid 
• 35924-04-0 4-Hydroxy-1-methyl-3,5-bis-(2-hydroxy-3,5-dimethyl-benzyl)-benzol 
• 172171-44-7 4-Methyl-2,6-bisphenol 
• 491573-62-7 2,6-bis{[(3,5-di-tert-butylbenzyl-2-hydroxy)(2-pyridylmethyl)amino]methyl}-4-methylphenol 
• 320714-00-9 ((2S,2'S)-((2-hydroxy-5-methyl-1,3-phenylene)bis(methylene))bis(pyrrolidine-1,2-diyl))bis(diphenylmethanol) 
• 389076-87-3 4-methyl-2,6-bis(diphenylphosphinomethyl)phenol P,P'-dioxide 

Relevant articles and documents

Models for Iron-Oxo Proteins. Structures and Properties of Fe(II)Fe(III), Zn(II)Fe(III), and Fe(II)Ga(III) Complexes with (μ-Phenoxo)bis(μ-carboxylato)dimetal Cores

A series of bimetallic complexes, X2 where BPMP is the anion of 2,6-bis-4-methylphenol, has been synthesized to provide models for binuclear metal-oxo centers in proteins (1, M = M' = Fe, R = C2H

Synthesis and properties of a heterobimetallic iron-manganese complex and its comparison with homobimetallic analogues

Heterobimetallic cofactors containing one manganese and one iron ion have recently been found within the di-metal carboxylate protein family. Herein we report the synthesis and characterization of three binuclear metal complexes with Fe-Fe, Mn-Mn, and Fe-Mn metal composition. All three complexes use the same ligand framework, the BPMP ligand (HBPMP = 2,6-bis[(bis (-2-pyridylmethyl)amine) methyl]-4-methylphenol)) with two additional acetate ligands bridging the two metals. In terms of stability towards metal exchange, the Fe-Mn is more stable than the Mn-Mn complex but less stable than the Fe-Fe complex. Cyclic voltammetry shows that the Fe-Mn complex behaves markedly different than the homobimetallic complexes. The Fe-Mn complex also shows higher reactivity with O2 than both the Fe-Fe and the Mn-Mn counterparts.

Nickel-catalyzed one-pot deoxygenation and reductive homocoupling of phenols via C-O activation using TCT reagent

A new method for C-O bond activation of phenolic compounds has been achieved using 2,4,6-trichloro-1,3,5-triazine to utilize in one-pot Ni-catalyzed deoxygenation and reductive homocoupling reactions. With this simple method, phenolic compounds were converted to their corresponding arenes or biaryl compounds under mild conditions. The introduced methodology has a broad scope and demonstrates good functional group compatibility.

Synthesis and characterization of oligonuclear Ru, Co and Cu oxidation catalysts

In this work, we report the preparation and crystal structures of three new oligonuclear complexes, Ru2(bbpmp)(μ-OAc)3 (4), [Co2(bbpmp)(μ-OAc)(μ-OMe)](PF6) (5), [Cu 4(Hbbpmp)2(μ-OAc)(H2O)2](OAc)(PF 6)2 (6) {H3bbpmp = 2,6-bis[(2-hydroxybenzyl)- (2-pyridylmethyl)aminomethyl]-4-methyl-phenol (3)}. The structures of the complexes were determined by single-crystal X-ray diffraction. The oxidation states of ruthenium, cobalt and copper in the complexes are +3, +3 and +2, respectively. In 4 and 5, RuIII and CoIII are coordinated to four oxygen and two nitrogen atoms in an octahedral geometry, while in 6, CuII adopts both octahedral (CuN2O4) and square-pyramidal (CuN2O3) geometry. The potential of the three complexes as oxidation catalysts has been investigated. Copyright