Cbz-R-3-amino-3-phenylpropan-1-ol

98%

Reagent Code: #104286
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CAS Number 888298-05-3

science Other reagents with same CAS 888298-05-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.34 g/mol
Formula C₁₇H₁₉NO₃
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Cbz-R-3-amino-3-phenylpropan-1-ol is widely used in organic synthesis, particularly in the preparation of pharmaceutical intermediates. It serves as a key building block in the development of chiral compounds, which are essential for creating enantiomerically pure drugs. This chemical is often employed in peptide synthesis, where the Cbz (carbobenzyloxy) group acts as a protective group for amines, ensuring selective reactions during complex molecular constructions. Additionally, it is utilized in the synthesis of bioactive molecules, including inhibitors and receptor modulators, due to its structural versatility. Its phenyl and amino groups make it a valuable precursor in the design of compounds targeting neurological and cardiovascular diseases.

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Test Parameter Specification
Purity (%) 97.5-100%
Optical Rotation (C = 1% in CH2Cl2) 42-48
Loss on Drying 0-0.5
Appearance White To Off-White Powder

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,260.00
inventory 200mg
10-20 days ฿774.00
inventory 5g
10-20 days ฿12,834.00

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Cbz-R-3-amino-3-phenylpropan-1-ol
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Cbz-R-3-amino-3-phenylpropan-1-ol is widely used in organic synthesis, particularly in the preparation of pharmaceutical intermediates. It serves as a key building block in the development of chiral compounds, which are essential for creating enantiomerically pure drugs. This chemical is often employed in peptide synthesis, where the Cbz (carbobenzyloxy) group acts as a protective group for amines, ensuring selective reactions during complex molecular constructions. Additionally, it is utilized in the synthesis of bioactive molecules, including inhibitors and receptor modulators, due to its structural versatility. Its phenyl and amino groups make it a valuable precursor in the design of compounds targeting neurological and cardiovascular diseases.
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