(R)-()-4-Methoxy-α-methylbenzylamine
98%
Reagent
Code: #71670
Alias
(R)-(+)-1-(4-methoxyphenyl)ethylamine; (R)-(+)-1-(4-methoxyphenyl)ethylamine, (R)-p-methoxy phenylethylamine, (R)-(+)-4-methoxy-α-methylbenzylamine
CAS Number
22038-86-4
blur_circular Chemical Specifications
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Molecular Information
Weight
151.21 g/mol
Formula
C₉H₁₃NO
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Registry Numbers
MDL Number
MFCD00671659
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Physical Properties
Boiling Point
65°C 0,4mm
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Storage & Handling
Density
1.024 g/mL at 20 °C(lit.)
Storage
room temperature, sealed
description Product Description
(R)-()-4-Methoxy-α-methylbenzylamine is primarily used as a chiral building block in the synthesis of various pharmaceuticals. Its chiral nature makes it valuable in the production of enantiomerically pure compounds, which are crucial for drugs that require specific stereochemistry to achieve desired biological activity. This compound is often employed in asymmetric synthesis, where it serves as a chiral auxiliary or ligand to induce stereoselectivity in chemical reactions. Additionally, it finds application in the development of agrochemicals and fine chemicals, where its structural framework contributes to the creation of biologically active molecules with enhanced efficacy and selectivity.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Purity (GC) | 98-100% |
Selective Chiral HPLC | 98-100 |
Specific Rotation (α20/D neat) | 30-34 |
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(R)-()-4-Methoxy-α-methylbenzylamine
(R)-()-4-Methoxy-α-methylbenzylamine is primarily used as a chiral building block in the synthesis of various pharmaceuticals. Its chiral nature makes it valuable in the production of enantiomerically pure compounds, which are crucial for drugs that require specific stereochemistry to achieve desired biological activity. This compound is often employed in asymmetric synthesis, where it serves as a chiral auxiliary or ligand to induce stereoselectivity in chemical reactions. Additionally, it finds application in the development of agrochemicals and fine chemicals, where its structural framework contributes to the creation of biologically active molecules with enhanced efficacy and selectivity.
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