(R)-(-)-1,2,3,4-Tetrahydro-1-naphthylamine
>99%, ee >98%
Reagent
Code: #71671
Alias
(R)-1,2,3,4-tetrahydro-1-naphthylamine; (R)-1-(1-amino)hydronaphthalene, (R)1-amino-1,2,3,4-tetra Hydronaphthalene
CAS Number
23357-46-2
blur_circular Chemical Specifications
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Molecular Information
Weight
147.22 g/mol
Formula
C₁₀H₁₃N
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Registry Numbers
MDL Number
MFCD00671629
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Physical Properties
Boiling Point
118-120°C 8mm
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Storage & Handling
Density
1.002
Storage
room temperature, sealed
description Product Description
(R)-(-)-1,2,3,4-Tetrahydro-1-naphthylamine is widely used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals. Its stereochemistry makes it valuable for creating enantiomerically pure compounds, which are essential in drug development to ensure efficacy and reduce side effects. It serves as an intermediate in the synthesis of various bioactive molecules, including central nervous system agents and cardiovascular drugs. Additionally, it is employed in asymmetric catalysis to facilitate the formation of chiral centers in complex organic molecules. Its applications extend to agrochemicals, where it contributes to the development of pesticides and herbicides with improved selectivity and activity.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | Colorless to light yellow to light orange clear liquid |
Purity | 98-100% |
Infrared Spectrum | Conforms to Structure |
Specific Rotation [α]20D (c=2, MeOH) | -28 |
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(R)-(-)-1,2,3,4-Tetrahydro-1-naphthylamine
(R)-(-)-1,2,3,4-Tetrahydro-1-naphthylamine is widely used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals. Its stereochemistry makes it valuable for creating enantiomerically pure compounds, which are essential in drug development to ensure efficacy and reduce side effects. It serves as an intermediate in the synthesis of various bioactive molecules, including central nervous system agents and cardiovascular drugs. Additionally, it is employed in asymmetric catalysis to facilitate the formation of chiral centers in complex organic molecules. Its applications extend to agrochemicals, where it contributes to the development of pesticides and herbicides with improved selectivity and activity.
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