Weight | 150.177 g/mol |
---|---|
Formula | C9H10O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
4'-Hydroxypropiophenone (70-70-2)
p-hydroxypropiophenone · 4-hydroxypropiophenone · para-hydroxypropiophenone
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- Laser flash photolysis study of the reactions of carbonyl triplets with phenols and photochemistry of p-hydroxypropiophenone (Journal of the American Chemical Society, 1981)
- Evaluation of a rapid radiometric differentiation test for the Mycobacterium tuberculosis complex by selective inhibition with p-nitro-alpha-acetylamino-beta-hydroxypropiophenone. (Journal of Clinical Microbiology, 1984)
- Synthesis of 14C Labeled 3-Methoxy-4-Hydroxy --(2-Methoxy-phenoxy)--Hydroxypropiophenone, a Lignin Model Compound (Holzforschung, 1981)
- Evaluation of the p-nitro-alpha-acetylamino-beta-hydroxypropiophenone differential test for identification of Mycobacterium tuberculosis complex. (Journal of Clinical Microbiology, 1985)
- p-Hydroxypropiophenone (PHP) and other so-called pituitary inhibitors (The Journal of Clinical Endocrinology and Metabolism, 1951)
- Propionylation of phenol to 4-hydroxypropiophenone over zeolite H-beta (Journal of Molecular Catalysis A-chemical, 2001)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - p-hydroxypropiophenone
- 4-hydroxypropiophenone
- para-hydroxypropiophenone
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SMILESCCC(=O)C1=CC=C(C=C1)O
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InChIKeyRARSHUDCJQSEFJ-UHFFFAOYSA-N
- Pubchem - 4'-Hydroxypropiophenone
- Wikipedia - paroxypropione
Paroxypropione is a synthetic nonsteroidal estrogen which has been used medically as an antigonadotropin in Spain and Italy but appears to no longer be marketed. It was first synthesized in 1902. The antigonadotropic properties of the drug were discovered in 1951 and it entered clinical use shortly thereafter.
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