Boc-Cys(Me)-OH

96%

Reagent Code: #104219
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CAS Number 16947-80-1

science Other reagents with same CAS 16947-80-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.30 g/mol
Formula C₉H₁₇NO₄S
badge Registry Numbers
MDL Number MFCD00076923
thermostat Physical Properties
Boiling Point 388.7°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used in peptide synthesis as a protected form of cysteine. The Boc (tert-butyloxycarbonyl) group serves as a protective group for the amino function, while the methyl group on the thiol side chain provides additional stability during the synthesis process. It is particularly useful in solid-phase peptide synthesis (SPPS) to prevent unwanted side reactions and ensure the correct formation of peptide bonds. The compound is also employed in the preparation of cysteine-containing peptides for research in biochemistry and pharmaceuticals, where precise control over the peptide structure is essential. Its application extends to the development of peptide-based drugs, where protecting groups are crucial for maintaining the integrity of the peptide chain during synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,034.00
inventory 250mg
10-20 days ฿837.00
inventory 5g
10-20 days ฿7,371.00
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Boc-Cys(Me)-OH
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This chemical is primarily used in peptide synthesis as a protected form of cysteine. The Boc (tert-butyloxycarbonyl) group serves as a protective group for the amino function, while the methyl group on the thiol side chain provides additional stability during the synthesis process. It is particularly useful in solid-phase peptide synthesis (SPPS) to prevent unwanted side reactions and ensure the correct formation of peptide bonds. The compound is also employed in the preparation of cysteine-containing peptides for research in biochemistry and pharmaceuticals, where precise control over the peptide structure is essential. Its application extends to the development of peptide-based drugs, where protecting groups are crucial for maintaining the integrity of the peptide chain during synthesis.
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