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品質等級
化驗
99%
形狀
solid
光學活性
[α]15/D +3°, c = 2 in dioxane
mp
153-155 °C (lit.)
SMILES 字串
COc1ccc2C3CC[C@@]4(C)C(CC[C@@]4(O)C#C)C3CCc2c1
InChI
1S/C21H26O2/c1-4-21(22)12-10-19-18-7-5-14-13-15(23-3)6-8-16(14)17(18)9-11-20(19,21)2/h1,6,8,13,17-19,22H,5,7,9-12H2,2-3H3/t17-,18-,19+,20+,21+/m1/s1
InChI 密鑰
IMSSROKUHAOUJS-MJCUULBUSA-N
基因資訊
human ... ESR1(2099)
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訊號詞
Warning
危險聲明
危險分類
Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
Dennis R Doose et al.
Epilepsia, 44(4), 540-549 (2003-04-12)
To study the pharmacokinetics of a combination oral contraceptive (OC) containing norethindrone and ethinyl estradiol during OC monotherapy, concomitant OC and topiramate (TPM) therapy, and concomitant OC and carbamazepine (CBZ) therapy in order to comparatively evaluate the pharmacokinetic interaction, which
Yuegang Zuo et al.
Chemosphere, 63(9), 1583-1590 (2005-11-26)
17alpha-Ethinylestradiol (EE2), a major constituent of common contraceptive pills, and three other estrogenic hormones, estrone (E1), 17beta-estradiol (E2) and mestranol (MeEE2) have been determined in Acushnet River Estuary seawater using a GC-MS technique. Among three estrogenic compounds detected, EE2 has
Yuegang Zuo et al.
Journal of chromatography. A, 1148(2), 211-218 (2007-04-03)
A rapid microwave-accelerated derivatization process for the GC-MS analysis of steroid estrogens, estrone (E1), 17beta-estradiol (E2), estriol (E3), 17alpha-ethynylestradiol (EE2) and mestranol (MeEE2), was developed. Under microwave irradiation, the five estrogenic hormones studied were simultaneously derivatized with N,O-bis(trimethylsilyl)trifluoroacetamide (BSTFA)+trimethylchlorosilane (TMCS)
A sesquineolignan with a spirodienone structure from Pinus sylvestris L.
Jari Sinkkonen et al.
Angewandte Chemie (International ed. in English), 46(22), 4148-4150 (2007-04-25)
Dóra Kovács et al.
Steroids, 77(11), 1075-1085 (2012-05-23)
Regioselective 1,3-dipolar cycloadditions of different aryl nitrile oxides to mestranol were carried out to furnish novel steroidal 17α-isoxazoles in good to excellent yields. Copper(I) was found to be an efficient catalyst, accelerating the intermolecular ring-closures and leading exclusively to 3,5-disubstituted
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