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115819

2,2′-Biphenol

Name: 2,2′-Biphenol
Brand: ALDRICH

99%

Synonym(s):

2,2′-Biphenyldiol, 2,2′-Dihydroxybiphenyl, 2,2′-Diphenol

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About This Item

Linear Formula:

HOC₆H₄C₆H₄OH

CAS Number:

1806-29-7

Molecular Weight:

186.21

UNSPSC Code:

12162002

NACRES:

NA.23

PubChem Substance ID:

24847240

EC Number:

217-303-0

Beilstein/REAXYS Number:

1638363

MDL number:

MFCD00002210

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Properties

Quality Level

100

assay

99%

form

solid

bp

315 °C (lit.)

mp

108-110 °C (lit.)

SMILES string

Oc1ccccc1-c2ccccc2O

InChI

1S/C12H10O2/c13-11-7-3-1-5-9(11)10-6-2-4-8-12(10)14/h1-8,13-14H

InChI key

IMHDGJOMLMDPJN-UHFFFAOYSA-N

Description

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

309.2 °F - closed cup - (External MSDS)

flash_point_c

154 °C - closed cup - (External MSDS)

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Broad spectrum antimicrobial biocides target the FabI component of fatty acid synthesis.

R J Heath et al.

The Journal of biological chemistry, 273(46), 30316-30320 (1998-11-07)

The broad spectrum antibacterial properties of 2-hydroxydiphenyl ethers have been appreciated for decades, and their use in consumer products is rapidly increasing. We identify the enoyl-acyl carrier protein reductase (fabI) component of the type II fatty acid synthase system as

Photochemical rearrangement of dibenzo[1,4]dioxins proceeds through reactive spirocyclohexadienone and biphenylquinone intermediates.

Sierra Rayne et al.

Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 4(11), 876-886 (2005-10-28)

Photochemical studies on a range of model dibenzo[1,4]dioxins were performed in aqueous and organic solutions. The compounds were found to undergo a photochemically initiated aryl-ether bond homolysis that yields reactive 2-spiro-6'-cyclohexa-2',4'-dien-1'-one and subsequent 2,2'-biphenylquinone intermediates. Under steady-state irradiation, the 2,2'-biphenylquinones

2,2'-Biphenols via protecting group-free thermal or microwave-accelerated Suzuki-Miyaura coupling in water.

Bernd Schmidt et al.

The Journal of organic chemistry, 78(17), 8680-8688 (2013-08-01)

User-friendly protocols for the protecting group-free synthesis of 2,2'-biphenols via Suzuki-Miyaura coupling of o-halophenols and o-boronophenol are presented. The reactions proceed in water in the presence of simple additives such as K2CO3, KOH, KF, or TBAF and with commercially available

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Global Trade Item Number

SKU	GTIN
115819-100G	04061838703637
115819-500G	04061833605387