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252018

2,6-Dibromophenol

99%

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About This Item

Linear Formula:
Br2C6H3OH
CAS Number:
608-33-3
Molecular Weight:
251.90
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24855174
EC Number:
210-161-0
Beilstein/REAXYS Number:
2043614
MDL number:
MFCD00002152
Assay:
99%
Form:
solid

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Quality Level

100

assay

99%

form

solid

bp

255-256 °C/740 mmHg (lit.)

mp

53-56 °C (lit.)

functional group

bromo

SMILES string

Oc1c(Br)cccc1Br

InChI

1S/C6H4Br2O/c7-4-2-1-3-5(8)6(4)9/h1-3,9H

InChI key

SSIZLKDLDKIHEV-UHFFFAOYSA-N

Gene Information

human ... ALOX12(239), ALOX15(246), GABRA1(2554)

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258164137715233277
2,6-Dibromophenol 99%

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2,6-Dibromophenol

2,4-Dibromophenol 95%

Sigma-Aldrich

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2,4-Dibromophenol

2,4,6-Tribromophenol 99%

Sigma-Aldrich

137715

2,4,6-Tribromophenol

2,6-Difluoropyridine 99%

Sigma-Aldrich

233277

2,6-Difluoropyridine

assay

99%

assay

95%

assay

99%

assay

99%

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

bp

255-256 °C/740 mmHg (lit.)

bp

154 °C/11 mmHg (lit.)

bp

282-290 °C/746 mmHg (lit.)

bp

124.5 °C/743 mmHg (lit.)

form

solid

form

solid

form

-

form

liquid

mp

53-56 °C (lit.)

mp

35-38 °C (lit.)

mp

90-94 °C (lit.)

mp

-

functional group

bromo

functional group

bromo

functional group

bromo

functional group

fluoro

General description

2,6-Dibromophenol has been isolated from a luminous marine enteropneust, Balanoglossus biminiensis and is responsible for the characteristic ″iodoform-like″ odor of these animals[1].

Application

2,6-Dibromophenol has been used in the preparation of 2-(2,6-dibromophenoxy)ethylbromide.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCQ4513
MKCN6944
MKCK6844
MKBJ7852V
MKBF2858

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R B Ashworth et al.
Science (New York, N.Y.), 155(3769), 1558-1559 (1967-03-24)
2,6-Dibromophenol has been isolated from a luminous marine enteropneust, Balanoglossus biminiensis, found on intertidal beach areas at Sapelo Island, Georgia. This compound, responsible for the characteristic "iodoform-like" odor of these animals, is present in relatively large amounts; the estimated quantity
Synthesis of arylpiperazines via palladium-catalysed aromatic amination reactions of bromoarenes with N- tert-butoxycarbonylpiperazine.
Kerrigan F, et al.
Tetrahedron Letters, 39(15), 2219-2222 (1998)
I Caroline Vaaland et al.
Chemosphere, 256, 126928-126928 (2020-05-23)
Phenols and trans-1,2-dihydro-1,2-diols are metabolites commonly formed in vivo in fish upon exposure to polycyclic aromatic hydrocarbons (PAHs). These metabolites are excreted via the bile and gas chromatography-mass spectrometry (GC-MS) analysis of bile is becoming more frequently used for evaluating PAH
M Schroeder et al.
Journal of agricultural and food chemistry, 56(7), 2485-2489 (2008-03-06)
Contaminating microorganisms such as Actinomycetes, Alicyclobacillus, and Chlostridium can generate off-flavors in apple juices. Such bacterial metabolites represent, besides phenol types such as guaiacol and 2,6-dibromophenol, a broad range of other chemicals, for example, geosmin, 2-methylisoborneol, or alpha-terpineol. A laccase
Noel Ferro et al.
Phytochemistry, 68(2), 237-250 (2006-11-28)
An computational-biostatistical approach, supported by ab initio optimizations of auxin-like molecules, was used to find biologically meaningful relationships between quantum chemical variables and fresh bioassay's data. It is proven that the auxin-like recognition requires different molecular assembling states. We suggest
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Global Trade Item Number

SKUGTIN
252018-10G04061825938103
252018-1G04061825938110

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