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| CAS No.: | 82517-12-2 |
|---|---|
| Name: | 5-Methyl-7-methoxyisoflavone |
| Article Data: | 3 |
| Molecular Structure: | |
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| Formula: | C17H14O3 |
| Molecular Weight: | 266.296 |
| Synonyms: | 7-Methoxy-5-methylisoflavone;Methoxyvone;4H-1-Benzopyran-4-one,7-methoxy-5-methyl-3-phenyl-; |
| EINECS: | 617-342-7 |
| Density: | 1.212 g/cm3 |
| Melting Point: | 116-120 °C |
| Boiling Point: | 449.3 °C at 760 mmHg |
| Flash Point: | 217.5 °C |
| Appearance: | white crystalline powder |
| Safety: | 24/25 |
| PSA: | 39.44000 |
| LogP: | 3.77700 |
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- 860579-89-1
1-(2-hydroxy-4-methoxy-6-methylphenyl)-2-phenylethan-1-one
- 122-51-0
orthoformic acid triethyl ester
- 82517-12-2
5-methyl-7-methoxyisoflavone
| Conditions | Yield |
|---|---|
| With piperidine; pyridine Yield given; |
- 4179-19-5
1,3-dimethoxy-5-methylbenzene
- 82517-12-2
5-methyl-7-methoxyisoflavone
| Conditions | Yield |
|---|---|
| Multi-step reaction with 2 steps 1: AlCl3 2: piperidine, pyridine View Scheme |
- 103-80-0
phenylacetyl chloride
- 82517-12-2
5-methyl-7-methoxyisoflavone
| Conditions | Yield |
|---|---|
| Multi-step reaction with 2 steps 1: AlCl3 2: piperidine, pyridine View Scheme |
- 64-67-5
diethyl sulfate
- 55338-30-2
7-hydroxy-5-methyl-3-phenyl-chromen-4-one
- 82517-12-2
5-methyl-7-methoxyisoflavone
| Conditions | Yield |
|---|---|
| With potassium carbonate In water |
| Conditions | Yield |
|---|---|
| at 20℃; Negishi Coupling; |
- 82517-12-2
5-methyl-7-methoxyisoflavone
| Conditions | Yield |
|---|---|
| With hydrazine hydrate In ethanol for 2h; Reflux; | 95% |
- 934-32-7
1H-benzimidazol-2-amine
- 82517-12-2
5-methyl-7-methoxyisoflavone
- 1179998-26-5
2-(2-hydroxy-4-methoxy-5-methylphenyl)-3-phenyl-pyrimido[1,2-a]benzimidazole
| Conditions | Yield |
|---|---|
| With sodium methylate In methanol at 65℃; for 8h; | 93% |
- 82517-12-2
5-methyl-7-methoxyisoflavone
- 55338-30-2
7-hydroxy-5-methyl-3-phenyl-chromen-4-one
| Conditions | Yield |
|---|---|
| With aluminium trichloride In benzene | 88% |
- 82517-12-2
5-methyl-7-methoxyisoflavone
- 1428876-28-1
9-methoxy-11-methyl-2H-phenanthro[9,10-c]pyrazole
| Conditions | Yield |
|---|---|
| Stage #1: 5-methyl-7-methoxyisoflavone With hydrazine hydrate In ethanol at 80℃; Stage #2: In ethanol; water at 20℃; for 4h; Inert atmosphere; Irradiation; | 86% |
- 50-01-1
guanidine hydrochloride
- 82517-12-2
5-methyl-7-methoxyisoflavone
- 1338784-55-6
2-amino-4-(2-hydroxy-4-methoxy-6-methylphenyl)-5-phenylpyrimidine
| Conditions | Yield |
|---|---|
| Stage #1: guanidine hydrochloride; 5-methyl-7-methoxyisoflavone With sodium hydroxide In ethanol for 4h; Reflux; Stage #2: With hydrogenchloride In ethanol; water | 82% |
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Chemistry
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IUPAC Name: 7-Methoxy-5-methyl-3-phenylchromen-4-one
Molecular Formula: C17H14O3
Molecular Weight: 266.29 g/mol
Canonical SMILES: CC1=CC(=CC2=C1C(=O)C(=CO2)C3=CC=CC=C3)OC
InChI: InChI=1S/C17H14O3/c1-11-8-13(19-2)9-15-16(11)17(18)14(10-20-15)12-6-4-3-5-7-12/h3-10H,1-2H3
Product Categories: Iso-Flavones
XLogP3-AA: 3.5
H-Bond Acceptor: 3
Surface Tension: 46.2 dyne/cm
Density: 1.212 g/cm3
Flash Point: 217.5 °C
Enthalpy of Vaporization: 70.79 kJ/mol
Boiling Point: 449.3 °C at 760 mmHg
Melting Point: 116-120 °C
Vapour Pressure of 5-Methyl-7-methoxyisoflavone (CAS NO.82517-12-2): 2.9E-08 mmHg at 25 °C
History
During the search for new anabolics in the 1970's, researchers strived to develop a compound that didn't have the pharmaceutical steroid status. The patent for methoxyflavone was first filed in 1977 by Chinoin, a Hungarian pharmaceutical company and leader in flavonoid research and knowledge. Then, in the 1980's, livestock producers introduced it as a new compound to increase lean mass in animals. Now, some 20 years later, with the end of its patent protection (which means anyone can copy the product, which is easy, since patents have to list exact manufacturing techniques), a new supplement, called methoxyisoflavone, popped onto the performance-supplement market... with no real science to back its claims.Unfortunately, patents don't mean a product works. They just mean the product is patented. In addition, methoxyflavones appear to have negative effects on important testosterone-conversion enzymes, whereby it inhibits the enzyme responsible for converting precursor hormones into testosterone. And, due to its similar structure to ipriflavone, it may even enhance the effects of estrogen in certain parts of the body (which isn't in the least bit beneficial for men trying to put on muscle mass).
Uses
5-Methyl-7-methoxyisoflavone (CAS NO.82517-12-2) is used for sports and fitness support (Enhancing Performance) and it is a chemical derivative of Ipriflavone, but it is marketed as a bodybuilding aid.
Safety Profile
Safety Statements of 5-Methyl-7-methoxyisoflavone (CAS NO.82517-12-2): 24/25
S24/25: Avoid contact with skin and eyes.
Specification
5-Methyl-7-methoxyisoflavone (CAS NO.82517-12-2), its Synonyms are Methyl-7-methoxy-isoflavone, 5- ; 7-Methoxy-5-methylisoflavone ; 5-Methyl-7-methoxyisoflavone 99+% . It is white crystalline powder.