115819
2,2′-Biphenol
99%
Synonym(s):
2,2′-Biphenyldiol, 2,2′-Dihydroxybiphenyl, 2,2′-Diphenol
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About This Item
Linear Formula:
HOC6H4C6H4OH
CAS Number:
Molecular Weight:
186.21
Beilstein:
1638363
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
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
Related Categories
Storage Class Code
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)
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Atsushi Kuwahara et al.
The Journal of organic chemistry, 70(2), 413-419 (2005-01-18)
The double N-arylation of primary amines with 2,2'-biphenylylene ditriflates was investigated for the synthesis of multisubstituted carbazoles. Palladium complexes supported by 2-dicyclohexylphosphino-2'-methylbiphenyl or Xantphos [4,5-bis(diphenylphosphino)-9,9-dimethylxanthene] were found to be efficient catalysts for the reaction. The catalysts allow the use of
V V Subrahmanyam et al.
Xenobiotica; the fate of foreign compounds in biological systems, 20(12), 1369-1378 (1990-12-01)
1. 14C-Phenol was metabolized by rat bone marrow homogenate and H2O2. The homogenate catalyst, however, was inactivated by preincubation with H2O2, presumably due to inactivation of the enzyme(s) involved in phenol metabolism. 2. The majority of the metabolized 14C-phenol was
Zwe-Ling Kong et al.
Bioorganic & medicinal chemistry letters, 15(1), 163-166 (2004-12-08)
The neolignans, magnolol 1 and honokiol 2 have been reported to inhibit the growth of several tumor cell lines in vitro and in vivo. The chemical structure of magnolol and honokiol consists of biphenyl skeleton with phenolic and allylic functionalities.
Christina DiMarco-Crook et al.
Journal of food science, 85(4), 1292-1301 (2020-03-08)
Chemoprevention strategies employing the use of multiple dietary bioactive components and their metabolites in combination offer advantages due to their low toxicity and potential synergistic interactions. Herein, for the first time, we studied the combination of curcumin and 3',4'-didemethylnobiletin (DDMN)
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
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