(S)-2-CBZ-AMINO-BUTANE-1,4-DIOL

97%

Reagent Code: #38347
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CAS Number 118219-23-1

science Other reagents with same CAS 118219-23-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.27 g/mol
Formula C₁₂H₁₇NO₄
thermostat Physical Properties
Boiling Point 461.0±45.0℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.220±0.06 g/cm3
Storage 2-8℃

description Product Description

This chemical is primarily used in the synthesis of chiral compounds and pharmaceutical intermediates. It serves as a key building block in the production of various biologically active molecules, particularly in the development of drugs targeting neurological and cardiovascular diseases. Its chiral nature makes it valuable for creating enantiomerically pure substances, which are crucial for ensuring the efficacy and safety of therapeutic agents. Additionally, it is employed in organic synthesis for constructing complex molecular structures with high precision. Its protective group (CBZ) allows for selective reactions, making it a versatile tool in medicinal chemistry and drug discovery.

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Test Parameter Specification
Appearance White Powder
Purity (%) 96.5-100%
Specific Rotation ([A]20/D (C=1, EtOH)) (deg) -34 to -28
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿15,831.00
inventory 1g
10-20 days ฿4,212.00

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(S)-2-CBZ-AMINO-BUTANE-1,4-DIOL
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This chemical is primarily used in the synthesis of chiral compounds and pharmaceutical intermediates. It serves as a key building block in the production of various biologically active molecules, particularly in the development of drugs targeting neurological and cardiovascular diseases. Its chiral nature makes it valuable for creating enantiomerically pure substances, which are crucial for ensuring the efficacy and safety of therapeutic agents. Additionally, it is employed in organic synthesis for cons

This chemical is primarily used in the synthesis of chiral compounds and pharmaceutical intermediates. It serves as a key building block in the production of various biologically active molecules, particularly in the development of drugs targeting neurological and cardiovascular diseases. Its chiral nature makes it valuable for creating enantiomerically pure substances, which are crucial for ensuring the efficacy and safety of therapeutic agents. Additionally, it is employed in organic synthesis for constructing complex molecular structures with high precision. Its protective group (CBZ) allows for selective reactions, making it a versatile tool in medicinal chemistry and drug discovery.

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