tert-Butyl3-(methoxymethyl)piperazine-1-carboxylate

97%

Reagent Code: #155703
fingerprint
CAS Number 1270982-05-2

science Other reagents with same CAS 1270982-05-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.3 g/mol
Formula C₁₁H₂₂N₂O₃
badge Registry Numbers
MDL Number MFCD19688481
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where piperazine rings are structural components. Its tert-butoxycarbonyl (Boc) protection allows for selective reactivity, making it valuable in multi-step organic syntheses. The methoxymethyl group enhances solubility and can act as a protecting group for alcohols or as a linker in prodrug strategies. Commonly employed in medicinal chemistry for drug discovery programs targeting central nervous system disorders, metabolic diseases, and infectious diseases due to the versatility of the piperazine scaffold.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,090.00
inventory 250mg
10-20 days ฿20,940.00
inventory 1g
10-20 days ฿64,270.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
tert-Butyl3-(methoxymethyl)piperazine-1-carboxylate
No image available

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where piperazine rings are structural components. Its tert-butoxycarbonyl (Boc) protection allows for selective reactivity, making it valuable in multi-step organic syntheses. The methoxymethyl group enhances solubility and can act as a protecting group for alcohols or as a linker in prodrug strategies. Commonly employed in medicinal chemistry for drug discover

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where piperazine rings are structural components. Its tert-butoxycarbonyl (Boc) protection allows for selective reactivity, making it valuable in multi-step organic syntheses. The methoxymethyl group enhances solubility and can act as a protecting group for alcohols or as a linker in prodrug strategies. Commonly employed in medicinal chemistry for drug discovery programs targeting central nervous system disorders, metabolic diseases, and infectious diseases due to the versatility of the piperazine scaffold.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...