1,1-Bis(benzyloxy)-N,N-dimethylmethanamine

95%

Reagent Code: #215723
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CAS Number 2016-04-8

science Other reagents with same CAS 2016-04-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.35 g/mol
Formula C₁₇H₂₁NO₂
badge Registry Numbers
MDL Number MFCD00014869
thermostat Physical Properties
Boiling Point 118-120 °C(lit.)
inventory_2 Storage & Handling
Density 1.045 g/cm3 at 25 °C(lit.)
Storage Room temperature, seal, inert gas

description Product Description

Used as a reagent in organic synthesis, particularly in the preparation of amine derivatives and functionalized intermediates. It serves as a dimethylaminomethylating agent, enabling the introduction of dimethylamino groups into various substrates. This compound is valuable in pharmaceutical and agrochemical industries for constructing nitrogen-containing molecules. Its benzyloxy groups can be cleaved under mild conditions, allowing for selective deprotection and further transformations in multi-step syntheses.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿3,530.00
5g
10-20 days ฿12,350.00
25g
10-20 days ฿43,230.00
1,1-Bis(benzyloxy)-N,N-dimethylmethanamine
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Used as a reagent in organic synthesis, particularly in the preparation of amine derivatives and functionalized intermediates. It serves as a dimethylaminomethylating agent, enabling the introduction of dimethylamino groups into various substrates. This compound is valuable in pharmaceutical and agrochemical industries for constructing nitrogen-containing molecules. Its benzyloxy groups can be cleaved under mild conditions, allowing for selective deprotection and further transformations in multi-step syn

Used as a reagent in organic synthesis, particularly in the preparation of amine derivatives and functionalized intermediates. It serves as a dimethylaminomethylating agent, enabling the introduction of dimethylamino groups into various substrates. This compound is valuable in pharmaceutical and agrochemical industries for constructing nitrogen-containing molecules. Its benzyloxy groups can be cleaved under mild conditions, allowing for selective deprotection and further transformations in multi-step syntheses.

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