N-CBz-guanidine

98%

Reagent Code: #219458
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CAS Number 16706-54-0

science Other reagents with same CAS 16706-54-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.20 g/mol
Formula C₉H₁₁N₃O₂
badge Registry Numbers
MDL Number MFCD09908206
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the preparation of biologically active compounds. It serves as a protected form of guanidine, allowing selective reactions at other functional sites in complex molecule assembly. Commonly applied in the development of pharmaceuticals, including protease inhibitors and other enzyme-targeted drugs. Its CBz (carbobenzyloxy) protection group is easily removed under mild conditions, making it valuable in peptide synthesis and medicinal chemistry workflows. Also utilized in the creation of arginine analogs and nitric oxide synthase research tools.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿610.00
inventory 1g
10-20 days ฿1,830.00
inventory 5g
10-20 days ฿6,410.00
inventory 25g
10-20 days ฿31,860.00
N-CBz-guanidine
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Used primarily as an intermediate in organic synthesis, especially in the preparation of biologically active compounds. It serves as a protected form of guanidine, allowing selective reactions at other functional sites in complex molecule assembly. Commonly applied in the development of pharmaceuticals, including protease inhibitors and other enzyme-targeted drugs. Its CBz (carbobenzyloxy) protection group is easily removed under mild conditions, making it valuable in peptide synthesis and medicinal chem

Used primarily as an intermediate in organic synthesis, especially in the preparation of biologically active compounds. It serves as a protected form of guanidine, allowing selective reactions at other functional sites in complex molecule assembly. Commonly applied in the development of pharmaceuticals, including protease inhibitors and other enzyme-targeted drugs. Its CBz (carbobenzyloxy) protection group is easily removed under mild conditions, making it valuable in peptide synthesis and medicinal chemistry workflows. Also utilized in the creation of arginine analogs and nitric oxide synthase research tools.

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