Cbz-S-3-amino-3-phenylpropan-1-ol

98%

Reagent Code: #60754
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CAS Number 869468-32-6

science Other reagents with same CAS 869468-32-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.34 g/mol
Formula C₁₇H₁₉NO₃
badge Registry Numbers
MDL Number MFCD16658906
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Cbz-S-3-amino-3-phenylpropan-1-ol is primarily used in organic synthesis as a building block for the preparation of more complex molecules. It serves as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of compounds with potential therapeutic effects. The presence of the Cbz (carbobenzyloxy) protecting group allows for selective deprotection, enabling controlled reactions in multi-step synthetic processes. This compound is also utilized in the study of enzyme inhibitors and receptor ligands, contributing to research in medicinal chemistry. Its structure makes it valuable for creating chiral molecules, which are essential in the production of enantiomerically pure drugs.

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Test Parameter Specification
Purity 97.5-100
Optical Rotation (c1, CH2Cl2) -47 to -43
Loss on Drying 0-0.5
Appearance Solid

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿760.00
inventory 1g
10-20 days ฿1,670.00
inventory 5g
10-20 days ฿5,250.00

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Cbz-S-3-amino-3-phenylpropan-1-ol
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Cbz-S-3-amino-3-phenylpropan-1-ol is primarily used in organic synthesis as a building block for the preparation of more complex molecules. It serves as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of compounds with potential therapeutic effects. The presence of the Cbz (carbobenzyloxy) protecting group allows for selective deprotection, enabling controlled reactions in multi-step synthetic processes. This compound is also utilized in the study of enzyme inhibitors and receptor ligands, contributing to research in medicinal chemistry. Its structure makes it valuable for creating chiral molecules, which are essential in the production of enantiomerically pure drugs.
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