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93601-86-6

  • Product Name:(S)-1,2,3,4-Tetrahydro-5-methoxy-N-propyl-2-naphthalenamine hydrochloride
  • Molecular Formula:C14H21NO.HCl
  • Molecular Weight:255.788
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Product Details

Purity:99%

Export (S)-1,2,3,4-Tetrahydro-5-methoxy-N-propyl-2-naphthalenamine 93601-86-6 In Stock In Bulk Supply

  • Molecular Formula:C14H21NO.HCl
  • Molecular Weight:255.788
  • Vapor Pressure:0-0Pa at 20-25℃ 
  • PSA:21.26000 
  • Density:1.19g/cm3 at 20℃ 
  • LogP:3.74500 

(S)-1,2,3,4-Tetrahydro-5-methoxy-N-propyl-2-naphthalenamine hydrochloride(Cas 93601-86-6) Usage

Chemical Properties

White Solid

Uses

Intermediate in the production of antipsychotic agents and antiparkinson medications.

Inventory In stock
Method Of Supply In bulk supply

Isomeric SMILES: CCCN[C@H]1CCC2=C(C1)C=CC=C2OC.Cl  
InChIKey: ZOKTXMBBTXQAIC-YDALLXLXSA-N  
InChI: InChI=1S/C14H21NO.ClH/c1-3-9-15-12-7-8-13-11(10-12)5-4-6-14(13)16-2;/h4-6,12,15H,3,7-10H2,1-2H3;1H/t12-;/m0./s1  

93601-86-6 Relevant articles

Preparation method of (S)-1, 2, 3, 4-tetrahydro-5-methoxy-N-propyl-2-naphthylamine hydrochloride

-

Paragraph 0040; 0060-0068, (2020/07/21)

The invention relates to a preparation m...

Enantioselective Synthesis of β-Aminotetralins via Chiral Phosphoric Acid-catalyzed Reductive Amination of β-Tetralones

Park, Do Young,Kim, Kyung-Hee,Cheon, Cheol-Hong

, p. 462 - 467 (2017/12/07)

A new protocol for the synthesis of chir...

New catalytic route for the synthesis of an optically active tetralone-derived amine for rotigotine

Cobley, Christopher J.,Evans, George,Fanjul, Tamara,Simmonds, Shaun,Woods, Amy

supporting information, p. 986 - 989 (2016/02/18)

Rotigotine is a launched drug for the tr...

Novel Process for the Preparation of Nitrogen Substituted Aminotetralins Derivatives

-

Paragraph 0233-0234, (2013/05/08)

The present invention provides an altern...

93601-86-6 Process route

(S)-1,2,3,4-tetrahydro-5-methoxy-N-propyl-naphthalen-2-ammonium (R)-2-(2-chlorophenyl)-2-hydroxyacetate
1352917-66-8

(S)-1,2,3,4-tetrahydro-5-methoxy-N-propyl-naphthalen-2-ammonium (R)-2-(2-chlorophenyl)-2-hydroxyacetate

(S)-(-)-(5-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)propylamine hydrochloride
93601-86-6

(S)-(-)-(5-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)propylamine hydrochloride

Conditions
Conditions Yield
With hydrogenchloride; In tetrahydrofuran; water; at 65 ℃; for 0.25h;
94%
With hydrogenchloride; In tetrahydrofuran; water; at 60 - 65 ℃; for 2.25h; Reflux;
94%
(S)-1,2,3,4-tetrahydro-5-methoxy-N-propyl-naphthalen-2-ammonium (S)-2-hydroxy-3-phenylpropionate
1352917-67-9

(S)-1,2,3,4-tetrahydro-5-methoxy-N-propyl-naphthalen-2-ammonium (S)-2-hydroxy-3-phenylpropionate

(S)-(-)-(5-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)propylamine hydrochloride
93601-86-6

(S)-(-)-(5-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)propylamine hydrochloride

Conditions
Conditions Yield
(S)-1,2,3,4-tetrahydro-5-methoxy-N-propyl-naphthalen-2-ammonium (S)-2-hydroxy-3-phenylpropionate; With sodium hydroxide; In 2-methyltetrahydrofuran; water; at 20 ℃;
With hydrogenchloride; In 2-methyltetrahydrofuran; water; at 60 ℃;
84%
(S)-1,2,3,4-tetrahydro-5-methoxy-N-propyl-naphthalen-2-ammonium (S)-2-hydroxy-3-phenylpropionate; With sodium hydroxide; In 2-methyltetrahydrofuran; water; at 20 ℃;
With hydrogenchloride; In 2-methyltetrahydrofuran; water; at 60 ℃;
84%

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