N,N′-Di-Boc-thiourea

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Reagent Code: #217068
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CAS Number 145013-05-4

science Other reagents with same CAS 145013-05-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.35 g/mol
Formula C₁₁H₂₀N₂O₄S
badge Registry Numbers
MDL Number MFCD03093917
thermostat Physical Properties
Melting Point 131-135°C (Lit.)
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of guanidine derivatives and heterocyclic compounds. It serves as a protected form of thiourea, allowing selective reactions in multi-step syntheses without interference from reactive functional groups. Commonly employed in pharmaceutical development for building nitrogen-containing scaffolds. Also utilized in the synthesis of agrochemicals and functional materials where controlled release of thiourea moiety is required. Its Boc-protected groups enhance solubility and stability in various reaction conditions, making it suitable for use in peptide chemistry and combinatorial library design.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿320.00
inventory 5g
10-20 days ฿1,300.00
inventory 25g
10-20 days ฿6,050.00
inventory 100g
10-20 days ฿24,030.00

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N,N′-Di-Boc-thiourea
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Used as a key intermediate in organic synthesis, particularly in the preparation of guanidine derivatives and heterocyclic compounds. It serves as a protected form of thiourea, allowing selective reactions in multi-step syntheses without interference from reactive functional groups. Commonly employed in pharmaceutical development for building nitrogen-containing scaffolds. Also utilized in the synthesis of agrochemicals and functional materials where controlled release of thiourea moiety is required. Its

Used as a key intermediate in organic synthesis, particularly in the preparation of guanidine derivatives and heterocyclic compounds. It serves as a protected form of thiourea, allowing selective reactions in multi-step syntheses without interference from reactive functional groups. Commonly employed in pharmaceutical development for building nitrogen-containing scaffolds. Also utilized in the synthesis of agrochemicals and functional materials where controlled release of thiourea moiety is required. Its Boc-protected groups enhance solubility and stability in various reaction conditions, making it suitable for use in peptide chemistry and combinatorial library design.

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