N-Boc-diethanolamine

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Reagent Code: #217401
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CAS Number 103898-11-9

science Other reagents with same CAS 103898-11-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.25 g/mol
Formula C₉H₁₉NO₄
badge Registry Numbers
MDL Number MFCD01862953
inventory_2 Storage & Handling
Density 1.085g/mL
Storage Room temperature, dry

description Product Description

Used as a protecting group reagent in organic synthesis, particularly in the pharmaceutical and agrochemical industries. Its primary application lies in the protection of amine functionalities during multi-step syntheses, where selective reactivity is crucial. The Boc (tert-butoxycarbonyl) group allows for mild deprotection conditions, making it compatible with a wide range of functional groups. N-Boc-diethanolamine serves as a building block in the preparation of complex molecules such as drug intermediates, especially in the synthesis of beta-blockers and other bioactive compounds. It is also utilized in the development of polymers and surfactants due to the presence of hydroxyl groups that can undergo further modification. Its stability under various reaction conditions enhances its utility in peptide chemistry and combinatorial synthesis.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿370.00
inventory 25g
10-20 days ฿1,760.00
inventory 500g
10-20 days ฿26,080.00
inventory 100g
10-20 days ฿6,130.00

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N-Boc-diethanolamine
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Used as a protecting group reagent in organic synthesis, particularly in the pharmaceutical and agrochemical industries. Its primary application lies in the protection of amine functionalities during multi-step syntheses, where selective reactivity is crucial. The Boc (tert-butoxycarbonyl) group allows for mild deprotection conditions, making it compatible with a wide range of functional groups. N-Boc-diethanolamine serves as a building block in the preparation of complex molecules such as drug intermedi

Used as a protecting group reagent in organic synthesis, particularly in the pharmaceutical and agrochemical industries. Its primary application lies in the protection of amine functionalities during multi-step syntheses, where selective reactivity is crucial. The Boc (tert-butoxycarbonyl) group allows for mild deprotection conditions, making it compatible with a wide range of functional groups. N-Boc-diethanolamine serves as a building block in the preparation of complex molecules such as drug intermediates, especially in the synthesis of beta-blockers and other bioactive compounds. It is also utilized in the development of polymers and surfactants due to the presence of hydroxyl groups that can undergo further modification. Its stability under various reaction conditions enhances its utility in peptide chemistry and combinatorial synthesis.

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