Boc-3-Phenylisoserine

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Reagent Code: #147958
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CAS Number 145514-62-1

science Other reagents with same CAS 145514-62-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 281.304 g/mol
Formula C₁₄H₁₉NO₅
badge Registry Numbers
MDL Number MFCD02259481
thermostat Physical Properties
Boiling Point 470.4℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.239g/ml
Storage 2-8℃, dry, sealed

description Product Description

Used in the synthesis of paclitaxel (Taxol), a potent anticancer drug, Boc-3-Phenylisoserine serves as a key chiral building block. Its protected functional groups allow selective coupling to the taxane core, enabling efficient construction of the C-13 side chain essential for biological activity. Widely employed in pharmaceutical research, it supports the development of taxane analogs with improved solubility, efficacy, or reduced resistance. Also utilized in solid-phase peptide synthesis and as an intermediate in preparing other bioactive molecules where stereochemistry and side-chain functionality are critical.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿1,540.00

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Boc-3-Phenylisoserine
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Used in the synthesis of paclitaxel (Taxol), a potent anticancer drug, Boc-3-Phenylisoserine serves as a key chiral building block. Its protected functional groups allow selective coupling to the taxane core, enabling efficient construction of the C-13 side chain essential for biological activity. Widely employed in pharmaceutical research, it supports the development of taxane analogs with improved solubility, efficacy, or reduced resistance. Also utilized in solid-phase peptide synthesis and as an inte

Used in the synthesis of paclitaxel (Taxol), a potent anticancer drug, Boc-3-Phenylisoserine serves as a key chiral building block. Its protected functional groups allow selective coupling to the taxane core, enabling efficient construction of the C-13 side chain essential for biological activity. Widely employed in pharmaceutical research, it supports the development of taxane analogs with improved solubility, efficacy, or reduced resistance. Also utilized in solid-phase peptide synthesis and as an intermediate in preparing other bioactive molecules where stereochemistry and side-chain functionality are critical.

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