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Merck
CN

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:
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Quality Level

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



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



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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
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.



全球贸易项目编号

货号GTIN
115819-100G04061838703637
115819-500G04061833605387