D70406
3,4-Dichlorophenol
99%
Synonym(s):
3,4-DCP
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About This Item
Linear Formula:
Cl2C6H3OH
CAS Number:
Molecular Weight:
163.00
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-450-5
Beilstein/REAXYS Number:
1907693
MDL number:
Assay:
99%
Form:
crystals
InChI key
WDNBURPWRNALGP-UHFFFAOYSA-N
InChI
1S/C6H4Cl2O/c7-5-2-1-4(9)3-6(5)8/h1-3,9H
SMILES string
Oc1ccc(Cl)c(Cl)c1
assay
99%
form
crystals
bp
~253 °C (lit.)
Quality Level
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Application
3,4-Dichlorophenol (3,4-DCP) is used in the synthesis of (Z)-5-arylmethylidene rhodanines as anti-methicillin-resistant Staphylococcus aureus (MRSA) agent. It can also be used in the preparation of 2-(3,4-dichlorophenoxy)-N-(2-morpholin-4-ylethyl)acetamide for the treatment of inflammatory pain.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
危险化学品
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The synthesis and SAR study of phenylalanine-derived (Z)-5-arylmethylidene rhodanines as anti-methicillin-resistant Staphylococcus aureus (MRSA) compounds.
Patel BA, et al.
Bioorganic & Medicinal Chemistry Letters, 23(20), 5523-5527 (2013)
Discovery of 2-(3, 4-dichlorophenoxy)-N-(2-morpholin-4-ylethyl) acetamide: A selective ?1 receptor ligand with antinociceptive effect.
Navarrete-Vazquez G, et al.
Biomedicine and Pharmacotherapy, 79(20), 284-293 (2016)
J H Carey et al.
Canadian journal of physiology and pharmacology, 62(8), 971-975 (1984-08-01)
The disappearance rates of 2,4- and 3,4-dichlorophenol in a small stream were studied and were shown to be first order with respect to either distance or time of flow. Both chlorophenols disappeared at approximately the same rate with average half-lives
F O Bryant et al.
Applied and environmental microbiology, 57(8), 2293-2301 (1991-08-01)
The reductive dechlorination of pentachlorophenol (PCP) was investigated in anaerobic sediments that contained nonadapted or 2,4- or 3,4-dichlorophenol (DCP)-adapted microbial communities. Adaptation of sediment communities increased the rate of conversion of 2,4- or 3,4-DCP to monochlorophenols (CPs) and eliminated the
Julien Michel et al.
Journal of the American Chemical Society, 131(18), 6356-6357 (2009-05-07)
There is great interest in molecules capable of inhibiting the interactions between p53 and its negative regulators hDM2 and hDMX, as these molecules have validated potential against cancers in which one or both oncoproteins are overexpressed. We reported previously that
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