![]() 5,6,7,8-Tetrahydro-2-naphthol structure
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Common Name | 5,6,7,8-Tetrahydro-2-naphthol | ||
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CAS Number | 1125-78-6 | Molecular Weight | 148.202 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 275.5±0.0 °C at 760 mmHg | |
Molecular Formula | C10H12O | Melting Point | 59-61 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 131.8±12.8 °C | |
Symbol |
![]() GHS07 |
Signal Word | Warning |
Photodegradation of the steroid hormones 17beta-estradiol (E2) and 17alpha-ethinylestradiol (EE2) in dilute aqueous solution.
Chemosphere 73(8) , 1216-23, (2008) The photochemical transformation of natural estrogenic steroid 17beta-estradiol (E2) and the synthetic oral contraceptive 17alpha-ethinylestradiol (EE2) has been studied in dilute non buffered aqueous solution (pH 5.5-6.0) upon monochromatic (254 nm) and poly... |
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An electron spin resonance study of o-semiquinones formed during the enzymatic and autoxidation of catechol estrogens.
J. Biol. Chem. 259(22) , 14018-22, (1984) Electron spin resonance spectroscopy has been used to demonstrate production of semiquinone-free radicals from the oxidation of the catechol estrogens 2- and 4-hydroxyestradiol and 2,6- and 4,6-dihydroxyestradiol. Radicals were generated either enzymatically ... |
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Estrone sulfonates as inhibitors of estrone sulfatase.
Steroids 62(4) , 346-50, (1997) In our continuing quest to design efficient inhibitors of estrone sulfatase activity and to assess the recognition of estrone sulfate surrogates by estrone sulfatase, we synthesized and evaluated several sulfonate derivatives of 5,6,7,8-tetrahydronaphth-2-ol ... |
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Non-radiative depletion of the excited electronic states of 9-cyanoanthracene in presence of tetrahydronaphthols.
Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 59(3) , 525-35, (2003) Both steady state and time resolved spectroscopic measurements reveal that the prime process involved in quenching mechanism of the lowest excited singlet (S1) and triplet (T1) states of the well known electron acceptor 9-Cyanoanthracene (9CNA) in presence of... |
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