产品名称
3-叔丁基苯酚, 99%
InChI key
CYEKUDPFXBLGHH-UHFFFAOYSA-N
InChI
1S/C10H14O/c1-10(2,3)8-5-4-6-9(11)7-8/h4-7,11H,1-3H3
SMILES string
CC(C)(C)c1cccc(O)c1
assay
99%
bp
125-130 °C/20 mmHg (lit.)
mp
44-46 °C (lit.)
Quality Level
Gene Information
mouse ... Esr1(13982)
Application
3-叔丁基苯酚已被用于研究酵母筛选中烷基在苯酚环上对烷基酚化合物的雌激素效能的影响。
General description
3-叔丁基苯酚在超临界二氧化碳溶剂中，在木炭负载的铑催化剂上发生立体选择性加氢。
Other Notes
含 4-叔丁基苯酚
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
228.2 °F - closed cup
flash_point_c
109 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Stereoselective hydrogenation of tert-butylphenols over charcoal-supported rhodium catalyst in supercritical carbon dioxide solvent.
Hiyoshi N, et al.
J. Catal., 252(1), 57-68 (2007)
E J Routledge et al.
The Journal of biological chemistry, 272(6), 3280-3288 (1997-02-07)
The ability of certain man-made chemicals to mimic the effects of natural steroid hormones and their potential to disrupt the delicate balance of the endocrine system in animals are of increasing concern. The growing list of reported hormone-mimics includes the
Tadashi Toyama et al.
Biodegradation, 21(2), 157-165 (2009-08-26)
A novel bacterium capable of utilizing 2-sec-butylphenol as the sole carbon and energy source, Pseudomonas sp. strain MS-1, was isolated from freshwater sediment. Within 30 h, strain MS-1 completely degraded 1.5 mM 2-sec-butylphenol in basal salt medium, with concomitant cell
Cynthia D Selassie et al.
Journal of medicinal chemistry, 48(23), 7234-7242 (2005-11-11)
In this comprehensive study on the caspase-mediated apoptosis-inducing effect of 51 substituted phenols in a murine leukemia cell line (L1210), we determined the concentrations needed to induce caspase activity by 50% (I50) and utilized these data to develop the following
Alfonso Pérez-Garrido et al.
Bioorganic & medicinal chemistry, 17(2), 896-904 (2008-12-06)
This paper reports a QSAR study for predicting the complexation of a large and heterogeneous variety of substances (233 organic compounds) with beta-cyclodextrins (beta-CDs). Several different theoretical molecular descriptors, calculated solely from the molecular structure of the compounds under investigation
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