3-Ethyl-2-methyl-2-(3-methylbutyl)-oxazolidine

Analytical Control

Reagent Code: #184158
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CAS Number 143860-04-2

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 185.31 g/mol
Formula C₁₁H₂₃NO
thermostat Physical Properties
Boiling Point 209 °C at 760 mmHg (lit.)
inventory_2 Storage & Handling
Density 0.872 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as a chiral auxiliary or intermediate in organic synthesis, particularly in the development of pharmaceuticals and fine chemicals. Its oxazolidine ring structure provides stereochemical control in asymmetric reactions, such as alkylations, aldol additions, and reductions. The presence of alkyl substituents enhances steric and electronic properties, making it suitable for directing selective transformations. Commonly employed in the synthesis of complex molecules where high enantioselectivity is required. Also finds use in the preparation of bioactive compounds and agrochemicals due to its stability and reactivity profile.

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inventory 100mg
10-20 days ฿22,000.00

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3-Ethyl-2-methyl-2-(3-methylbutyl)-oxazolidine
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Used as a chiral auxiliary or intermediate in organic synthesis, particularly in the development of pharmaceuticals and fine chemicals. Its oxazolidine ring structure provides stereochemical control in asymmetric reactions, such as alkylations, aldol additions, and reductions. The presence of alkyl substituents enhances steric and electronic properties, making it suitable for directing selective transformations. Commonly employed in the synthesis of complex molecules where high enantioselectivity is requ

Used as a chiral auxiliary or intermediate in organic synthesis, particularly in the development of pharmaceuticals and fine chemicals. Its oxazolidine ring structure provides stereochemical control in asymmetric reactions, such as alkylations, aldol additions, and reductions. The presence of alkyl substituents enhances steric and electronic properties, making it suitable for directing selective transformations. Commonly employed in the synthesis of complex molecules where high enantioselectivity is required. Also finds use in the preparation of bioactive compounds and agrochemicals due to its stability and reactivity profile.

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