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(1S)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline

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(1S)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline Basic information

Product Name:
(1S)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline
Synonyms:
  • Solifenacin Related Compound 11
  • (S)-1,2,3,4- four-1- phenylhydrogenisoquinoline
  • Solifenacin Succinate interMediate F
  • (S)-1-phenyl-1,2,3,4-tetrahydroisoquinoline, Solifenacin intermediate
  • Solifenacin Impurity A
  • (S)-1,2,3,4-Tetrahydro-1-phenylisoquinoline,99%e.e.
  • (S)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline
  • (1S)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline in stock Factory
CAS:
118864-75-8
MF:
C15H15N
MW:
209.29
EINECS:
1806241-263-5
Product Categories:
  • Other APIs
  • Aromatics
  • API intermediates
  • Chiral Reagents
  • Heterocycles
  • Isotope Labeled Compounds
  • Aromatics Compounds
Mol File:
118864-75-8.mol
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(1S)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline Chemical Properties

Melting point:
80-82°C
Boiling point:
338°C
Density 
1.065
Flash point:
167°C
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
solubility 
Chloroform (Slightly), Dichloromethane (Slightly), Methanol (Slightly)
form 
Solid
pka
8.91±0.40(Predicted)
color 
White to Off-White
CAS DataBase Reference
118864-75-8(CAS DataBase Reference)
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Safety Information

HS Code 
2933.49.7000
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(1S)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline Usage And Synthesis

Chemical Properties

White Solid

Uses

Labelled Solifenacin intermediate

Uses

Solifenacin (S676700) intermediate.

Uses

(1S)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline has been used as a lead compound for the development of drugs with dopamine β-hydroxylase inhibitory activity. In vitro studies have shown that 1-phenyl-1,2,3,4-tetrahydro-isoquinoline inhibits human serum dopamine β-hydroxylase and can be used to study the possible role of this enzyme in Parkinson's disease. 

(1S)-1-Phenyl-1,2,3,4-tetrahydroisoquinolineSupplier

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