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Details
Manufacturer supply 4-(4-hydroxy-3-methoxyphenyl)butan-2-ol 39728-80-8 with sufficient stock and high standard
- Molecular Formula: C11H16 O3
- Molecular Weight: 196.246
- Vapor Pressure: 2.51E-05mmHg at 25°C
- Boiling Point: 344.4°Cat760mmHg
- Flash Point: 162.1°C
- PSA： 49.69000
- Density: 1.117g/cm3
- LogP: 1.71420
4-(4-hydroxy-3-methoxyphenyl)butan-2-ol(Cas 39728-80-8) Usage
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General Description |
4-(4-hydroxy-3-methoxyphenyl)butan-2-ol, also known as HHPB, is a chemical compound with the molecular formula C13H18O3. It is an organic compound that belongs to the class of phenolic alcohols. HHPB is commonly found in various natural sources, such as plants and fruits, and is known for its antioxidant properties. This chemical is used in the production of pharmaceuticals, cosmetics, and food products due to its ability to scavenge free radicals and prevent oxidative damage. It is also being studied for its potential health benefits, such as anti-inflammatory and anti-cancer properties. HHPB is considered to be a safe and beneficial compound with a wide range of applications in various industries. |
InChI:InChI=1/C11H16O3/c1-8(12)3-4-9-5-6-10(13)11(7-9)14-2/h5-8,12-13H,3-4H2,1-2H3
39728-80-8 Relevant articles
Zingerone in the flower of passiflora maliformis attracts an australian fruit fly, bactrocera jarvisi (Tryon)
Cameron, Donald N. S.,Cheesman, Jodie,De Faveri, Stefano G.,Hanssen, Benjamin L.,Jamie, Ian M.,Park, Soo Jean,Taylor, Phillip W.
, (2020)
Passiflora maliformis is an introduced p...
Phenyl trimethyl ammonium tribromide mediated robust one-pot synthesis of spiro-oxacycles-an economic route-stereoselective synthesis of oxaspirohexacyclodieneones
Sarkar, Debayan,Ghosh, Manoj Kumar,Rout, Nilendri
, p. 7883 - 7898 (2016/08/30)
This paper entails the first recognition...
Synthesis of raspberry and ginger ketones by nickel boride-catalyzed hydrogenation of 4-arylbut-3-en-2-ones
Bandarenko, Mikhail,Kovalenko, Vitaly
, p. 885 - 888 (2014/11/08)
Raspberry and ginger ketones have been s...
Glycerol/Hypophosphorous acid and PhSeSePh: An efficient and selective system for reactions in the carbon-carbon double bond of (E)-chalcones
Mesquita, Katiu?cia D.,Waskow, Bianca,Schumacher, Ricardo F.,Perin, Gelson,Jacob, Raquel G.,Alves, Diego
, p. 1261 - 1269 (2014/08/05)
We describe herein our results for the r...
39728-80-8 Process route
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1080-12-2,22214-42-2
(E)-4-(4-hydroxy-3-methoxyphenyl)but-3-ene-2-one
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39728-80-8
3-hydroxy-1-(4-hydroxy-3-methoxyphenyl)butane
| Conditions | Yield |
|---|---|
|
Multi-step reaction
with
2
steps
1: H2
/ Pd/C / ethyl acetate
2: 91 percent / NaBH4
/ ethanol
With
sodium tetrahydroborate; hydrogen;
palladium on activated charcoal;
In
ethanol; ethyl acetate;
|
|
|
Multi-step reaction
with
2
steps
1: H2
/ 10 percent Pd/C / ethyl acetate
2: H2
/ 10 percent Pd/C / ethyl acetate
With
hydrogen;
palladium on activated charcoal;
In
ethyl acetate;
|
|
|
Multi-step reaction
with
3
steps
1: 86 percent / H2
/ Raney nickel / acetone
2: 84 percent / phenol, hexamethyldisilazane / benzene / Heating
3: 1.) lithium di-isopropylamide, hexanal, 2.) 2M HCl / 1.) -78 deg C, 1 h, THF, 2.) ether
With
hydrogenchloride; hydrogen; hexanal; 1,1,1,3,3,3-hexamethyl-disilazane; lithium diisopropyl amide; phenol;
nickel;
In
acetone; benzene;
|
-
-
1080-12-2
Dehydrozingerone
-
-
122-48-5
4-(4-hydroxy-3-methoxyphenyl)-2-butanone
-
-
39728-80-8
3-hydroxy-1-(4-hydroxy-3-methoxyphenyl)butane
| Conditions | Yield |
|---|---|
|
With
palladium 10% on activated carbon; hydrogen; acetic acid;
In
methanol;
at 20 ℃;
for 24h;
|
37%
58% |
|
With
ethanol; palladium;
Hydrogenation;
|
39728-80-8 Upstream products
-
1080-12-2
Dehydrozingerone
-
56700-87-9
4-(3-methoxy-4-trimethylsilyloxyphenyl)butan-2-one
-
66-25-1
hexanal
-
64-17-5
ethanol
39728-80-8 Downstream products
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1443152-51-9
(R)-4-(4'-hydroxy-3'-methoxyphenyl)-2-butyl acetate
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1450832-91-3
(S)-4-(4'-hydroxy-3'-methoxyphenyl)-2-butyl acetate
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1443152-50-8
(S)-4-(4'-acetyloxy-3'-methoxyphenyl)-2-butanol
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960357-43-1
4-(2-benzyl-4-hydroxy-5-methoxyphenyl)butan-2-one
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