115819
2,2′-联苯酚
99%
别名:
2,2′-二羟基联苯, 2,2′-联苯二酚, 2,2′-联苯酚
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关于此项目
线性分子式:
HOC6H4C6H4OH
化学文摘社编号:
分子量:
186.21
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
217-303-0
Beilstein/REAXYS Number:
1638363
MDL number:
产品名称
2,2′-联苯酚, 99%
InChI key
IMHDGJOMLMDPJN-UHFFFAOYSA-N
InChI
1S/C12H10O2/c13-11-7-3-1-5-9(11)10-6-2-4-8-12(10)14/h1-8,13-14H
SMILES string
Oc1ccccc1-c2ccccc2O
assay
99%
form
solid
bp
315 °C (lit.)
mp
108-110 °C (lit.)
Quality Level
存储类别
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
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)
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
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
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
M Sondossi et al.
Applied and environmental microbiology, 70(1), 174-181 (2004-01-09)
The purpose of this investigation was to examine the capacity of the biphenyl catabolic enzymes of Comamonas testosteroni B-356 to metabolize dihydroxybiphenyls symmetrically substituted on both rings. Data show that 3,3'-dihydroxybiphenyl is by far the preferred substrate for strain B-356.
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