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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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:
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
Riadh Sahnoun et al.
The journal of physical chemistry. A, 110(7), 2440-2447 (2006-02-17)
The S-R enantiomerization processes of 2,2'-biphenol (biphenol) have been investigated using density functional theory (DFT). Five isomers for biphenol were identified: I0, which is the most stable isomer; I1a and I1b, which are formed by a restricted rotation of one
T Kuhnigk et al.
Journal of basic microbiology, 37(3), 205-211 (1997-01-01)
The capability of the intestinal flora from the gut of xylophagous termites of degrading lignin model compounds was investigated. Different dimeric lignin model compounds-degrading bacteria were obtained from the hindgut flora of Mastotermes darwiniensis Froggatt, Reticulitermes santonensis Feytaud, Nasutitermes nigriceps
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.
W A Prütz et al.
International journal of radiation biology and related studies in physics, chemistry, and medicine, 44(2), 183-196 (1983-08-01)
Phenoxyl radicals generated pulse radiolytically by the reaction of N.3 with Gly-Tyr decay biomolecularly (2k = 4.7 X 10(8)M-1 s-1) with efficient formation of 2,2'-dimers, which enolize rapidly (k = 2.7 X 10(4) s-1) to produce the 2,2'-biphenolic product. The
Alaa S Amin et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 96, 541-547 (2012-07-07)
A solid phase extraction technique is proposed for preconcentration and speciation of chromium in natural waters using spectrophotometric analysis. The procedure is based on sorption of chromium(III) as 4-(2-benzothiazolylazo)2,2'-biphenyldiol complex on dextran-type anion-exchange gel (Sephadex DEAE A-25). After reduction of
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