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- CasNo152623-93-3
- Purity99%
Location:Home > Pharmaceutical
Cosmetics Grade 6-(2-aminopropyl)-2,3-dihydrobenzofuran 152623-93-3 For Sale with Good Price
- Molecular Formula:C11H15NO
- Molecular Weight:177.246
- Vapor Pressure:0.00179mmHg at 25°C
- Refractive Index:1.565
- Boiling Point:292.868 °C at 760 mmHg
- Flash Point:134.233 °C
- PSA：35.25000
- Density:1.088 g/cm3
- LogP:2.21150
6-(2-aminopropyl)-2,3-dihydrobenzofuran(Cas 152623-93-3) Usage
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General Description |
6-(2-aminopropyl)-2,3-dihydrobenzofuran is a chemical compound that belongs to the class of benzofuran compounds. It consists of a benzene ring fused with a furan ring and a 2-aminopropyl side chain. 6-(2-aminopropyl)-2,3-dihydrobenzofuran is also known as 6-APDB and is classified as a designer drug or research chemical. It is not approved for medical use and is primarily used for recreational purposes, particularly as a psychedelic drug. 6-APDB is known to produce effects such as euphoria, hallucinations, and altered perception, making it appealing to some individuals for its psychoactive properties. However, |
InChI:InChI=1/C11H15NO/c1-8(12)6-9-2-3-10-4-5-13-11(10)7-9/h2-3,7-8H,4-6,12H2,1H3
152623-93-3 Relevant articles
Successful use of a novel lux i-Amylose-1 chiral column for enantioseparation of “legal highs” by HPLC
Kadkhodaei, Kian,Kadisch, Marlene,Schmid, Martin G.
, p. 42 - 52 (2019/11/14)
Bath salts, fumigations, cleaners and ai...
Enantiomeric separation of Novel Psychoactive Substances by capillary electrophoresis using (+)-18-crown-6-tetracarboxylic acid as chiral selector
H?gele, Johannes S.,Schmid, Martin G.
, p. 1019 - 1026 (2018/07/29)
In the recent years, hundreds of Novel P...
Enantioselective potential of polysaccharide-based chiral stationary phases in supercritical fluid chromatography
Kucerova, Gabriela,Kalikova, Kveta,Tesarova, Eva
supporting information, p. 239 - 246 (2017/05/29)
The enantioselective potential of two po...
Synthesis and Pharmacological Examination of Benzofuran, Indan, and Tetralin Analogues of 3,4-(Methylenedioxy)amphetamine
Monte, Aaron P.,Marona-Lewicka, Danuta,Cozzi, Nicholas V.,Nichols, David E.
, p. 3700 - 3706 (2007/10/02)
Benzofuran, indan and tetrahydronaphthal...
152623-93-3 Process route
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152623-93-3
6-(2-aminopropyl)-2,3-dihydrobenzofuran
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152623-93-3
1‐(2,3‐dihydro‐1‐benzofuran‐6‐yl)propan‐2‐amine
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152623-93-3
1‐(2,3‐dihydro‐1‐benzofuran‐6‐yl)propan‐2‐amine
Conditions
| Conditions | Yield |
|---|---|
|
With
isopropylamine; trifluoroacetic acid;
In
tetrahydrofuran; methanol; isopropyl alcohol;
at 35 ℃;
under 103432 Torr;
Reagent/catalyst;
Solvent;
Resolution of racemate;
Supercritical conditions;
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|
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With
(2R,3R,11R,12R)-(+)-18-crown-6-2,3,11,12-tetracarbonic acid;
In
aq. buffer;
at 20 ℃;
for 0.25h;
pH=2.1;
enantioselective reaction;
Resolution of racemate;
|
|
|
With
Lux i-Amylose-1 column;
In
hexane; diethylamine; isopropyl alcohol;
at 20 ℃;
Resolution of racemate;
|
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152623-93-3
6-(2-aminopropyl)-2,3-dihydrobenzofuran
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152623-93-3
1‐(2,3‐dihydro‐1‐benzofuran‐6‐yl)propan‐2‐amine
-
-
152623-93-3
1‐(2,3‐dihydro‐1‐benzofuran‐6‐yl)propan‐2‐amine
Conditions
| Conditions | Yield |
|---|---|
|
With
isopropylamine; trifluoroacetic acid;
In
tetrahydrofuran; methanol; isopropyl alcohol;
at 35 ℃;
under 103432 Torr;
Reagent/catalyst;
Solvent;
Resolution of racemate;
Supercritical conditions;
|
|
|
With
(2R,3R,11R,12R)-(+)-18-crown-6-2,3,11,12-tetracarbonic acid;
In
aq. buffer;
at 20 ℃;
for 0.25h;
pH=2.1;
enantioselective reaction;
Resolution of racemate;
|
|
|
With
Lux i-Amylose-1 column;
In
hexane; diethylamine; isopropyl alcohol;
at 20 ℃;
Resolution of racemate;
|
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