• R-tetrahydropapaverine hcl

R-tetrahydropapaverine hcl

  • CasNo:54417-53-7
  • Purity:99%

Product Details;

CasNo: 54417-53-7

Molecular Formula: C20H25NO4

Hot Sale Top Purity Reliable Quality R-tetrahydropapaverine hcl 54417-53-7

  • Molecular Formula:C20H25NO4
  • Molecular Weight:379.884
  • Vapor Pressure:3.23E-09mmHg at 25°C 
  • Refractive Index:1.549 
  • Boiling Point:475.8 °C at 760 mmHg 
  • Flash Point:202.7 °C 
  • PSA:48.95000 
  • Density:1.12 g/cm3 
  • LogP:4.28130 

R-Tetrahydropapaverine(Cas 54417-53-7) Usage

Application

R-tetrahydropapaverine HCl is a useful research chemical.

Consumer Uses

ECHA has no public registered data indicating whether or in which chemical products the substance might be used. ECHA has no public registered data on the routes by which this substance is most likely to be released to the environment.

InChI:InChI=1/C20H25NO4/c1-22-17-6-5-13(10-18(17)23-2)9-16-15-12-20(25-4)19(24-3)11-14(15)7-8-21-16/h5-6,10-12,16,21H,7-9H2,1-4H3/t16-/m1/s1

54417-53-7 Relevant articles

Half-quantity resolution method of racemic mixture of tetrahydroisoquinoline type compound

-

Paragraph 0040-0043; 0046; 0058, (2017/10/13)

The invention discloses a half-quantity ...

Organocatalytic Enantioselective Pictet-Spengler Approach to Biologically Relevant 1-Benzyl-1,2,3,4-Tetrahydroisoquinoline Alkaloids

Ruiz-Olalla, Andrea,Würdemann, Martien A.,Wanner, Martin J.,Ingemann, Steen,Van Maarseveen, Jan H.,Hiemstra, Henk

, p. 5125 - 5132 (2015/05/27)

(Figure Presented) A general procedure f...

PROCESS FOR THE RESOLUTION OF ISOQUINOLINE DERIVATIVES

-

Page/Page column 5, (2010/12/29)

A process for the resolution of racemic ...

PROCESS FOR THE RESOLUTION OF ISOQUINOLINE DERIVATIVES

-

Page/Page column 9-10, (2009/10/21)

A process for the resolution of racemic ...

54417-53-7 Process route

1,2,3,4-tetrahydro-1-(3,4-dimethoxybenzyl)-6,7-dimethoxyisoquinoline hydrochloride
6429-04-5,66820-84-6

1,2,3,4-tetrahydro-1-(3,4-dimethoxybenzyl)-6,7-dimethoxyisoquinoline hydrochloride

(R)-tetrahydropapaverine hydrochloride
54417-53-7,66820-84-6

(R)-tetrahydropapaverine hydrochloride

Conditions
Conditions Yield
With N-acetyl-D-leucine; (R)-N-acetylphenylalanin; In water; toluene; acetonitrile; at 4 - 70 ℃; for 24.92h; Reagent/catalyst;
83.25%
(-) N-norlaudanosine
50896-90-7

(-) N-norlaudanosine

(R)-tetrahydropapaverine hydrochloride
54417-53-7,66820-84-6

(R)-tetrahydropapaverine hydrochloride

Conditions
Conditions Yield
With hydrogenchloride; In ethanol; water; at 20 ℃; for 1h;
99.8 % ee
With hydrogenchloride; In ethanol; at 20 ℃; for 1h;
99.8 % ee

54417-53-7 Upstream products

  • 6957-27-3
    6957-27-3

    3,4-dihydropapaverine

  • 50896-90-7
    50896-90-7

    (-) N-norlaudanosine

  • 74-88-4
    74-88-4

    methyl iodide

  • 6429-04-5
    6429-04-5

    1,2,3,4-tetrahydro-1-(3,4-dimethoxybenzyl)-6,7-dimethoxyisoquinoline hydrochloride

54417-53-7 Downstream products

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    1075726-74-7

    (1R)-1-[(3,4-dimethoxyphenyl)-methyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-2-aminocarbonylethyl-isoquinoline oxalate

  • 1075726-79-2
    1075726-79-2

    (1R)-1-[(3,4-dimethoxyphenyl)-methyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-2-benzyloxycarbonylethyl-isoquinoline oxalate

  • 1075726-76-9
    1075726-76-9

    (1R)-1-[(3,4-dimethoxyphenyl)-methyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-2-methoxycarbonylethyl-isoquinoline oxalate

  • 1075726-71-4
    1075726-71-4

    (1R)-1-[(3,4-dimethoxyphenyl)-methyl]-1,2,3,4-tetrahydro-6,7-dimethoxy-2-tert-butoxycarbonylethyl-isoquinoline oxalate

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