(S)-(−)-α-Methylbenzylamine
>99.0%(GC)
Reagent
Code: #71651
Alias
(S)-(-)-α-Methylbenzylamine ;S-1-Phenylethylamine, S(-)-α-Phenylethylamine, Methylbenzylamine
CAS Number
2627-86-3
Properties
Reminder: The product can only be used for scientific research purposes
blur_circular Chemical Specifications
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Molecular Information
Weight
121.18 g/mol
Formula
C₈H₁₁N
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Registry Numbers
EC Number
220-098-0
MDL Number
MFCD00064406
thermostat
Physical Properties
Melting Point
-10 °C
Boiling Point
187 °C(lit.)
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Storage & Handling
Density
0.94 g/mL at 25 °C(lit.)
Storage
2~8°C
description Product Description
(S)-(−)-α-Methylbenzylamine is widely used as a chiral resolving agent in organic synthesis. It is particularly valuable for separating racemic mixtures of carboxylic acids and other chiral compounds through the formation of diastereomeric salts. This process allows for the isolation of enantiomerically pure substances, which is crucial in the pharmaceutical industry for producing drugs with specific stereochemistry. Additionally, it serves as a chiral building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its application extends to asymmetric synthesis, where it acts as a chiral auxiliary or ligand in catalytic reactions, enhancing enantioselectivity. This compound is also utilized in research and development for studying stereochemical effects and developing new chiral catalysts.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | Colorless liquid |
Specific Rotation (α20D, neat) | -41 |
Purity | 99 |
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(S)-(−)-α-Methylbenzylamine
(S)-(−)-α-Methylbenzylamine is widely used as a chiral resolving agent in organic synthesis. It is particularly valuable for separating racemic mixtures of carboxylic acids and other chiral compounds through the formation of diastereomeric salts. This process allows for the isolation of enantiomerically pure substances, which is crucial in the pharmaceutical industry for producing drugs with specific stereochemistry. Additionally, it serves as a chiral building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its application extends to asymmetric synthesis, where it acts as a chiral auxiliary or ligand in catalytic reactions, enhancing enantioselectivity. This compound is also utilized in research and development for studying stereochemical effects and developing new chiral catalysts.
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