(S)-(-)-α,4-Dimethylbenzylamine
95%
Reagent
Code: #71679
Alias
(S)-1-(4-methylphenyl)ethylamine; (S)-(-)-1-p-methylphenylethylamine
CAS Number
27298-98-2
blur_circular Chemical Specifications
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Molecular Information
Weight
135.21 g/mol
Formula
C₉H₁₃N
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Registry Numbers
MDL Number
MFCD00145246
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Physical Properties
Boiling Point
205 °C(lit.)
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Storage & Handling
Density
0.919 g/mL at 25 °C(lit.)
Storage
room temperature, sealed
description Product Description
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of enantiomerically pure drugs. It serves as a key intermediate in the development of active pharmaceutical ingredients (APIs) for treatments targeting central nervous system disorders, cardiovascular diseases, and other therapeutic areas. Its chiral nature allows for the creation of compounds with high stereochemical purity, enhancing drug efficacy and reducing side effects. Additionally, it is employed in asymmetric synthesis and catalysis, contributing to the development of advanced chemical processes in organic chemistry.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Purity | 94.5-100 |
Refractive Index N20D | 1.52-1.522 |
Specific Gravity (2020) | 0.935-0.937 |
Optical Purity (EE) | 99 (GLC) |
Specific rotation (α20D neat) | -38 to -34 |
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(S)-(-)-α,4-Dimethylbenzylamine
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of enantiomerically pure drugs. It serves as a key intermediate in the development of active pharmaceutical ingredients (APIs) for treatments targeting central nervous system disorders, cardiovascular diseases, and other therapeutic areas. Its chiral nature allows for the creation of compounds with high stereochemical purity, enhancing drug efficacy and reducing side effects. Additionally, it is employed in asymmetric synthesis and catalysis, contributing to the development of advanced chemical processes in organic chemistry.
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