N-Cbz-S-4-Hydroxyphenylglycine

95%

Reagent Code: #218917
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CAS Number 26787-76-8

science Other reagents with same CAS 26787-76-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 301.29 g/mol
Formula C₁₆H₁₅NO₅
badge Registry Numbers
MDL Number MFCD09756649
thermostat Physical Properties
Boiling Point 552 °C(Predicted)
inventory_2 Storage & Handling
Density 1.356 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of β-lactam antibiotics, particularly in the preparation of side chains for penicillins and cephalosporins. Its protected hydroxyl and amino groups allow selective reactions in multi-step organic syntheses. The Cbz group facilitates easy deprotection under mild conditions, making it valuable in peptide coupling and semisynthetic antibiotic development. Also employed in asymmetric synthesis due to its stereocenter, contributing to the production of optically active pharmaceuticals.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,090.00
inventory 1g
10-20 days ฿3,190.00
inventory 5g
10-20 days ฿6,010.00
N-Cbz-S-4-Hydroxyphenylglycine
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Used as a chiral building block in the synthesis of β-lactam antibiotics, particularly in the preparation of side chains for penicillins and cephalosporins. Its protected hydroxyl and amino groups allow selective reactions in multi-step organic syntheses. The Cbz group facilitates easy deprotection under mild conditions, making it valuable in peptide coupling and semisynthetic antibiotic development. Also employed in asymmetric synthesis due to its stereocenter, contributing to the production of opticall

Used as a chiral building block in the synthesis of β-lactam antibiotics, particularly in the preparation of side chains for penicillins and cephalosporins. Its protected hydroxyl and amino groups allow selective reactions in multi-step organic syntheses. The Cbz group facilitates easy deprotection under mild conditions, making it valuable in peptide coupling and semisynthetic antibiotic development. Also employed in asymmetric synthesis due to its stereocenter, contributing to the production of optically active pharmaceuticals.

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