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B73406

6-Bromo-2-naphthol

Name: 6-Bromo-2-naphthol
Brand: ALDRICH

97%

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About This Item

Linear Formula:

BrC₁₀H₆OH

CAS Number:

15231-91-1

Molecular Weight:

223.07

NACRES:

NA.22

PubChem Substance ID:

24891987

UNSPSC Code:

12352100

EC Number:

239-279-0

MDL number:

MFCD00004081

Assay:

97%

Form:

powder

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Properties

Quality Level

100

assay

97%

form

powder

mp

122-124 °C (lit.)

SMILES string

Oc1ccc2cc(Br)ccc2c1

InChI

1S/C10H7BrO/c11-9-3-1-8-6-10(12)4-2-7(8)5-9/h1-6,12H

InChI key

YLDFTMJPQJXGSS-UHFFFAOYSA-N

Description

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

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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Visualizing antibody-catalyzed retro-aldol-retro-Michael reactions.

F Tanaka et al.

Bioorganic & medicinal chemistry letters, 11(22), 2983-2986 (2001-10-26)

We developed a visible detection system for antibody-catalyzed retro-aldol-retro-Michael reactions. Aldolase antibody 38C2 catalyzed the reaction of substrate 1 to provide 6-bromo-2-napthol that forms a visible colored azo dye with diazonium salts. This system has potential for the screening of

Room temperature phosphorescence of 6-bromo-2-naphthol in micelles of poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) block copolymers and in their mixed aggregates with sodium dodecyl sulfate.

K Nakashima et al.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 58(1), 123-128 (2002-01-26)

Room temperature phosphorescence (RTP) of 6-bromo-2-naphthol has been investigated in aqueous micellar solutions of poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) block copolymers as well as in their mixed aggregates with sodium dodecyl sulfate. RTP of the phosphorophor was enhanced to some extent

Ligand- and Solvent-Tuned Chemoselective Carbonylation of Bromoaryl Triflates.

Chaoren Shen et al.

Chemistry (Weinheim an der Bergstrasse, Germany), 23(54), 13369-13378 (2017-06-27)

The palladium-catalyzed chemoselective carbonylation of bromoaryl triflates is reported. The selective C-Br bond versus C-OTf (OTf=triflate) bond functionalization can be remarkably tuned by the combination of the ligand [4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (Xantphos) vs. 1,1'-bis(diphenylphosphino)ferrocene (DPPF)] and the solvent (toluene vs. DMSO). The

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Global Trade Item Number

SKU	GTIN
B73406-25G	04061833441770
B73406-100G	04061832883410