312753-53-0
- Product Name:5,6-Diethyl-2,3-dihydro-1H-inden-2-amine hydrochloride
- Molecular Formula:C13H19N.HCl
- Purity:99%
- Molecular Weight:225.762
Product Details;
CasNo: 312753-53-0
Molecular Formula: C13H19N.HCl
Chinese Manufacturer Supply High Purity 5,6-Diethyl-2,3-dihydro-1H-inden-2-amine hydrochloride 312753-53-0 Safe Shipping
- Molecular Formula:C13H19N.HCl
- Molecular Weight:225.762
- Vapor Pressure:0.00285mmHg at 25°C
- Melting Point:>250 °C
- Boiling Point:285.2 °C at 760 mmHg
- Flash Point:127.6 °C
- PSA:26.02000
- LogP:3.73960
5,6-Diethyl-2,3-dihydro-1H-inden-2-amine hydrochloride(Cas 312753-53-0) Usage
Uses |
5,6-Diethyl-2,3-dihydro-1H-inden-2-amine Hydrochloride acts as a reagent in the synthetic preparation of quinolinone compounds and it’s formulations in combination with corticosteroids for treatment of airway disorder. |
Synthesis |
Preparation 4-5,6-Diethyl-indan-2-ylamine Hydrochloride 5,6-Diethyl-3-oxime-1H-indene-1,2(3H)-dione (4.5 g) is added to a mixture of acetic acid (150 mL), and concentrated sulphuric acid (4.5 mL). Pd/C5% (1.5 g) is added, the reaction mixture degassed with nitrogen, and hydrogenated for 5 hours. The catalyst is then removed by filtration, the pH brought to pH 10 with 4M NaOH, and the solution extracted with chloroform. The organic phase is dried with magnesium sulphate, and the solvent removed in vacuo. The residue is redisolved in a minimum amount of ether, and HCl saturated ether added. The white precipitate is filtered and dried to yield the HCl salt of 5,6-diethyl-indan-2-ylamine, a compound of formula XVII where R3, R4 and R7 are H, R5 and R6 are each CH3CH2-, R30 is hydrogen and n is 1. 5,6-Diethyl-indan-2-ylamine Hydrochloride. |
InChI:InChI=1/C13H19N.ClH/c1-3-9-5-11-7-13(14)8-12(11)6-10(9)4-2;/h5-6,13H,3-4,7-8,14H2,1-2H3;1H
312753-53-0 Relevant articles
Method for preparing 5,6-diethyl-2,3-dihydro-1H-indene-2-amino hydrochloride
-
, (2019/10/01)
The invention relates to a novel synthes...
Preparation method of indacaterol intermediate
-
, (2018/11/22)
The invention provides a preparation met...
The identification of indacaterol as an ultralong-acting inhaled β2-adrenoceptor agonist
Baur, Fran?ois,Beattie, David,Beer, David,Bentley, David,Bradley, Michelle,Bruce, Ian,Charlton, Steven J.,Cuenoud, Bernard,Ernst, Roland,Fairhurst, Robin A.,Faller, Bernard,Farr, David,Keller, Thomas,Fozard, John R.,Fullerton, Joe,Garman, Sheila,Hatto, Julia,Hayden, Claire,He, Handan,Howes, Colin,Janus, Diana,Jiang, Zhengjin,Lewis, Christine,Loeuillet-Ritzler, Frederique,Moser, Heinz,Reilly, John,Steward, Alan,Sykes, David,Tedaldi, Lauren,Trifilieff, Alexandre,Tweed, Morris,Watson, Simon,Wissler, Elke,Wyss, Daniel
supporting information; experimental part, p. 3675 - 3684 (2010/07/16)
Following a lipophilicity-based hypothes...
An efficient and economical synthesis of 5,6-diethyl-2,3-dihydro-1H-inden- 2-amine hydrochloride
Prashad, Mahavir,Hu, Bin,Har, Denis,Repic, Oljan,Blacklock, Thomas J.,Lohse, Olivier
, p. 135 - 141 (2012/12/21)
An efficient and economical synthesis of...
312753-53-0 Process route
-
C13H17N3
- 312753-53-0
5,6-diethyl-2,3-dihydro-1H-inden-2-amine hydrochloride
Conditions | Yield |
---|---|
C13H17N3; With palladium 10% on activated carbon; hydrogen; In methanol; under 3800.26 Torr; Autoclave;
With hydrogenchloride; In ethyl acetate;
|
92% |
-
C15H21NO
- 312753-53-0
5,6-diethyl-2,3-dihydro-1H-inden-2-amine hydrochloride
Conditions | Yield |
---|---|
With hydrogenchloride; In water; for 10h; Reflux;
|
92.6% |
312753-53-0 Upstream products
-
601487-90-5
N-(5,6-diethyl-2,3-dihydro-1H-inden-2-yl)-2,2,2-trifluoroacetamide
-
312753-70-1
5,6-diethyl-2,3-dihydro-1H-inden-2-amine
-
193756-44-4
N-(2,3-dihydro-1H-inden-2-yl)-2,2,2-trifluoroacetamide
-
601487-87-0
N-(5-acetyl-2,3-dihydro-1H-inden-2-yl)-2,2,2-trifluoroacetamide
312753-53-0 Downstream products
-
312753-06-3
indacaterol
-
435273-75-9
(R)-8-(benzyloxy)-5-[2-[(5,6-diethyl-2,3-dihydro-1H-indole-2-yl)amino]-1-hydroxyethyl]quinolin-2(1H)-one
-
312753-70-1
5,6-diethyl-2,3-dihydro-1H-inden-2-amine
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753498-25-8
indacaterol maleate
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