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Sigma-Aldrich

Bis(5-chlor-2-hydroxyphenyl)methan

95%

Synonym(e):

Dichlorophen

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About This Item

Lineare Formel:
CH2[C6H3(Cl)OH]2
CAS-Nummer:
97-23-4
Molekulargewicht:
269.12
Beilstein:
1884514
EG-Nummer:
202-567-1
MDL-Nummer:
MFCD00002322
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24848095
NACRES:
NA.22

Assay

95%

Form

powder

mp (Schmelzpunkt)

168-172 °C (lit.)

Löslichkeit

95% ethanol: soluble 1g/g
methanol: soluble
petroleum ether: soluble
toluene: very slightly soluble
water: insoluble

SMILES String

Oc1ccc(Cl)cc1Cc2cc(Cl)ccc2O

InChI

1S/C13H10Cl2O2/c14-10-1-3-12(16)8(6-10)5-9-7-11(15)2-4-13(9)17/h1-4,6-7,16-17H,5H2

InChIKey

MDNWOSOZYLHTCG-UHFFFAOYSA-N

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Allgemeine Beschreibung

Bis(5-chloro-2-hydroxyphenyl)methane is a fungicide and is very effective against many celluloytic fungi, such as Penicillium, Aspergillus,Cladosporium and Trichoderma sp. It is a phenolic pesticide and undergoes photodegradation in the presence of visible-light absorber photosensitizer riboflavin.

Anwendung

Bis(5-chloro-2-hydroxyphenyl)methane can be used as a starting material to synthesize methyl aluminium-(2,2′-methylene-p-chloro-bisphenoxide), which is used as a catalyst for the ring opening polymerization (ROP) of cyclic esters. It can also be used as an organic building block to prepare phosphomides substituted with aminoacid esters for various biological studies.

Haftungsausschluss

The product is not intended for use as a biocide under global biocide regulations, including but not limited to US EPA′s Federal Insecticide Fungicide and Rodenticide Act, European Biocidal Products Regulation, Canada’s Pest Management Regulatory Agency, Turkey’s Biocidal Products Regulation, Korea’s Consumer Chemical Products and Biocide Safety Management Act (K-BPR) and others.

Piktogramme

Exclamation markEnvironment
GHS07,GHS09

Signalwort

Warning

Gefahreneinstufungen

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Reaction of methyl aluminium-(2, 2?-methylene-p-chloro-bisphenoxide) with 2, 2?-di (hydroxymethyl) biphenyl: A new aluminium complex bearing two kinds of diolate ligands
Ziemkowska W, et al.
Journal of Organometallic Chemistry, 693(3), 369-373 (2008)
Synthesis and antimicrobial activity of 2,10-dichloro-6-substituted amino acid ester12H-dibenzo[d,g][1,3,2]dioxaphosphocin-6-oxides
BS Kumar, et al.
Bulgarian Chemical Communications, 41(4), 422-426 (2009)
F J Verhagen et al.
Applied and environmental microbiology, 64(9), 3225-3231 (1998-09-03)
Higher fungi have a widespread capacity for biosynthesis of organohalogens. Commonly occurring chloroaromatic fungal metabolites can end up in anaerobic microniches at the boundary of fungal colonies and wetland soils. The aim of this study was to investigate the environmental
Antoine Ghauch et al.
Journal of hazardous materials, 164(2-3), 665-674 (2008-09-30)
Palladium, ruthenium and silver were investigated as catalysts for the dechlorination of dichlorophen (DCP, 2,2'-methylenebis(4-chlorophenol)), an antimicrobial and anthelmintic agent largely used as algicide, fungicide and bactericide. Experiments were undertaken under oxic and anoxic conditions for experimental durations up to
Ki-Bong Oh et al.
Bioorganic & medicinal chemistry letters, 19(3), 945-948 (2008-12-23)
A series of halophenols was prepared by the reaction of bis(hydroxyphenyl)methanes with effective halogenating agents such as bromine and sulfuryl chloride. One of these compounds, a biologically active halophenol--2,2',3,3'-tetrabromo-4,4',5,5'-tetrahydroxydiphenylmethane (1)--frequently isolated from red algae, was synthesized for the first time.
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