- Transformation of steroids by Trichoderma hamatumBartmanska, Agnieszka; Dmochowska-Gladysz, Jadwiga, Enzyme and Microbial Technology, 2007, 40(6), 1615-1621
Cas no 21661-22-3 (6alpha-hydroxyandrosta-1,4-diene-3,17-dione)
21661-22-3 structure
Product Name:6alpha-hydroxyandrosta-1,4-diene-3,17-dione
CAS No:21661-22-3
MF:C19H24O3
MW:300.392066001892
CID:2057900
Update Time:2025-04-21
6alpha-hydroxyandrosta-1,4-diene-3,17-dione Chemical and Physical Properties
Names and Identifiers
-
- 6alpha-hydroxyandrosta-1,4-diene-3,17-dione
- 7alpha-hydroxyandrosta-1,4-diene-3,17-dione
-
- Inchi: 1S/C19H24O3/c1-18-7-5-11(20)9-15(18)16(21)10-12-13-3-4-17(22)19(13,2)8-6-14(12)18/h5,7,9,12-14,16,21H,3-4,6,8,10H2,1-2H3
- InChI Key: JCJRNURQXRSFJI-UHFFFAOYSA-N
- SMILES: CC12C(=O)CCC1C1CC(C3C(C1CC2)(C)C=CC(=O)C=3)O
Computed Properties
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 22
- XLogP3: 1.888
6alpha-hydroxyandrosta-1,4-diene-3,17-dione Production Method
Production Method 1
Reaction Conditions
1.1 Solvents: Acetone , Water ; 8 d, 27 °C
Reference
6alpha-hydroxyandrosta-1,4-diene-3,17-dione Raw materials
6alpha-hydroxyandrosta-1,4-diene-3,17-dione Preparation Products
6alpha-hydroxyandrosta-1,4-diene-3,17-dione Related Literature
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Hailing Chen,Lu Yin,Meng Liu,Laibing Wang,Michiya Fujiki,Wei Zhang RSC Adv., 2019,9, 4849-4856
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Huiying Xu,Lu Zheng,Yu Zhou,Bang-Ce Ye Analyst, 2021,146, 5542-5549
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M. Sheykhan,S. Khani,S. Shaabanzadeh,M. Joafshan Green Chem., 2017,19, 5940-5948
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Muniyandi Sankaralingam,So Hyun Jeon,Yong-Min Lee,Mi Sook Seo,Wonwoo Nam Dalton Trans., 2016,45, 376-383
-
Huifang Yang,Haoran Guo,Peidong Fan,Xinpan Li,Wenlu Ren,Rui Song Nanoscale, 2020,12, 7024-7034
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