(R)-(-)-1,2,3,4-Tetrahydro-1-naphthylamine

>99%, ee >98%

Reagent Code: #71671
label
Alias (R)-1,2,3,4-tetrahydro-1-naphthylamine; (R)-1-(1-amino)hydronaphthalene, (R)1-amino-1,2,3,4-tetra Hydronaphthalene
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CAS Number 23357-46-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 147.22 g/mol
Formula C₁₀H₁₃N
badge Registry Numbers
MDL Number MFCD00671629
thermostat Physical Properties
Boiling Point 118-120°C 8mm
inventory_2 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

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿530.00
inventory 25g
10-20 days ฿8,180.00
inventory 5g
10-20 days ฿1,960.00
(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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