- CasNo 15462-91-6
- Purity 99%
Location:Home > Pharmaceutical
Quality manufacturer supply 3-[2-(3,4-dimethoxybenzoyl)-4,5-dimethoxyphenyl]pentan-2-one 15462-91-6 in stock with high standard
- Molecular Formula: C22H26 O6
- Molecular Weight: 386.445
- Vapor Pressure: 2.91E-12mmHg at 25°C
- Melting Point: 156-157 °C
- Boiling Point: 552.7°Cat760mmHg
- Flash Point: 239.8°C
- PSA: 71.06000
- Density: 1.124g/cm3
- LogP: 4.03460
3-[2-(3,4-dimethoxybenzoyl)-4,5-dimethoxyphenyl]pentan-2-one(Cas 15462-91-6) Usage
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General Description |
3-[2-(3,4-dimethoxybenzoyl)-4,5-dimethylphenyl]pentan-2-one is a chemical compound. The detailed structural specification suggests that it has multiple functional groups, including a pentan-2-one, or a pentanone, which is a type of ketone; a 3,4-dimethoxybenzoyl, which suggests a benzoic acid ester derivative with two methoxy groups; and a 4,5-dimethylphenyl, which is a phenyl group substituted with two methyl groups. It's not a common or widely-used chemical, and as such, there’s limited information available about its properties, uses, or safety. Therefore, any handling or use of it should be done with utmost caution, preferably under the guidance of a trained professional. It falls in the scientific realm of organic chemistry--the study of structures, properties, composition, reactions, and synthesis of organic compounds consisting of carbon atoms. |
InChI:InChI=1/C22H26O6/c1-7-15(13(2)23)16-11-20(27-5)21(28-6)12-17(16)22(24)14-8-9-18(25-3)19(10-14)26-4/h8-12,15H,7H2,1-6H3
15462-91-6 Relevant articles
holds the non-rope to divide method for the preparation of intermediates
-
, (2017/02/24)
The invention relates to a preparation m...
One-pot synthesis of 2,3-benzodiazepines from arynes and β-diketones
Okuma, Kentaro,Tanabe, Yukiko,Itoyama, Ryoichi,Nagahora, Noriyoshi,Shioji, Kosei
supporting information, p. 1260 - 1262 (2013/10/22)
Novel one-pot synthesis of 2,3-benzodiaz...
PROCESS FOR THE PREPARATION OF 3-[2-(3,4-DIMETHOXYBENZOYL)-4,5- DIMETHOXYPHENYL] -PENTAN-2-ONE
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Page 17, (2008/06/13)
The invention relates to a new process f...
PROCESS FOR THE PREPARATION OF 3-[2-(3,4-DIMETHOXY-BENZOYL)-4,5-DIMETHOXY-PHENYL]-PENTAN-2-ONE
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Page 14-15, (2010/02/07)
The invention relates to a process for t...
15462-91-6 Process route
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4483-47-0,15161-79-2,22688-51-3,22688-52-4,22688-53-5,62211-17-0
(+-)-1r -ethyl-3c -(3,4-dimethoxy-phenyl)-5,6-dimethoxy-2t -methyl-indan
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64-19-7,77671-22-8
acetic acid
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15462-91-6
3-[2-(3,4-dimethoxybenzoyl)-4,5-dimethoxyphenyl]pentan-2-one
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7249-36-7
2-(3,4-Dimethoxy-benzoyl)-4,5-dimethoxy-benzoic acid
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93-07-2
Veratric acid
| Conditions | Yield |
|---|---|
|
at 15 - 20 ℃;
|
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4483-47-0
1-(3,4-dimethoxy-phenyl)-3-ethyl-5,6-dimethoxy-2-methyl-indane
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15462-91-6
3-[2-(3,4-dimethoxybenzoyl)-4,5-dimethoxyphenyl]pentan-2-one
| Conditions | Yield |
|---|---|
|
With
hydrogenchloride; dihydrogen peroxide; acetic acid; copper(II) oxide;
In
water;
at 3 - 25 ℃;
for 10h;
Reagent/catalyst;
Temperature;
|
88.2%
|
15462-91-6 Upstream products
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186581-53-3
diazomethane
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82005-37-6
1-ethyl-3-(3,4-dimethoxy-phenyl)-5,6-dimethoxy-2-methyl-indene
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2029-86-9
1-(3,4-dimethoxyphenyl)-6,7-dimethoxy-4-ethyl-3-methylisochroman
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64-19-7
acetic acid
15462-91-6 Downstream products
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1616-49-5
4-ethyl-3-methyl-6,7-dimethoxy-1-(3,4-dimethoxyphenyl)isoquinoline
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114920-22-8
4-ethyl-1-(3,4-dimethoxy-phenyl)-6,7-dimethoxy-3-methyl-isoquinoline-2-oxide
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22345-47-7
tofisopam
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98352-06-8
4-Ethyl-6,7-dimethoxy-1-(3,4-dimethoxyphenyl)-3-methylisoquinoline-N-p-toluenesulphonylimine
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