Butestrol | |
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Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C16H18O2[1] |
Molecular mass | 242.31 g/mol[1] |
Predicted LogP | 4.1[1] |
Chirality | absolute[2] |
Identifiers [] | |
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IUPAC name | 4-[(2R,3R)-3-(4-hydroxyphenyl)butan-2-yl]phenol[1] |
SMILES | C[C@@H](C1=CC=C(C=C1)O)[C@@H](C)C2=CC=C(C=C2)O[1] |
InChI | InChI=1S/C16H18O2/c1-11(13-3-7-15(17)8-4-13)12(2)14-5-9-16(18)10-6-14/h3-12,17-18H,1-2H3/t11-,12-/m1/s1[1] |
InChIKey | GDUYFVYTXYOMSJ-VXGBXAGGSA-N[1] |
Dosing |
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Butestrol
Butestrol (also known as DL-Butestrol, 5776-76-1, racemic-Butestrol, racemic-Butoestrol, 15542-16-2, D-Dma, L-Dma, DL-Dma, (+)-4,4'-(1,2-Dimethylethylene)diphenol or (-)-4,4'-(1,2-Dimethylethylene)diphenol)
Chemistry
Stereochemistry
Butestrol is a absolute mixture