(R)-()-α-Methylbenzyl isocyanate

99%

Reagent Code: #230050
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CAS Number 33375-06-3

science Other reagents with same CAS 33375-06-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 147.17 g/mol
Formula C₉H₉NO
badge Registry Numbers
MDL Number MFCD00063015
thermostat Physical Properties
Boiling Point 55-56°C 2.5mm Hg (Lit.)
inventory_2 Storage & Handling
Density 1.0270g/ml
Storage 2-8°C

description Product Description

Used primarily as a chiral derivatizing agent in the resolution of enantiomers, especially in the separation of racemic mixtures of amines and alcohols. Its reactivity with nucleophiles allows the formation of diastereomeric ureas or carbamates, which can be easily separated by conventional techniques such as chromatography or crystallization. Widely applied in asymmetric synthesis and pharmaceutical research for obtaining enantiomerically pure compounds. Also serves as an intermediate in the preparation of chiral auxiliaries, catalysts, and optically active isocyanates for fine chemical manufacturing.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,220.00
inventory 5g
10-20 days ฿3,400.00
inventory 25g
10-20 days ฿9,630.00
inventory 100g
10-20 days ฿30,840.00

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(R)-()-α-Methylbenzyl isocyanate
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Used primarily as a chiral derivatizing agent in the resolution of enantiomers, especially in the separation of racemic mixtures of amines and alcohols. Its reactivity with nucleophiles allows the formation of diastereomeric ureas or carbamates, which can be easily separated by conventional techniques such as chromatography or crystallization. Widely applied in asymmetric synthesis and pharmaceutical research for obtaining enantiomerically pure compounds. Also serves as an intermediate in the preparation

Used primarily as a chiral derivatizing agent in the resolution of enantiomers, especially in the separation of racemic mixtures of amines and alcohols. Its reactivity with nucleophiles allows the formation of diastereomeric ureas or carbamates, which can be easily separated by conventional techniques such as chromatography or crystallization. Widely applied in asymmetric synthesis and pharmaceutical research for obtaining enantiomerically pure compounds. Also serves as an intermediate in the preparation of chiral auxiliaries, catalysts, and optically active isocyanates for fine chemical manufacturing.

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