tert-Butyl (4-iodo-2-methoxypyridin-3-yl)carbamate

≥95%

Reagent Code: #113321
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CAS Number 162709-20-8

science Other reagents with same CAS 162709-20-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 350.15 g/mol
Formula C₁₁H₁₅IN₂O₃
badge Registry Numbers
MDL Number MFCD22200465
thermostat Physical Properties
Boiling Point 340.0±42.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

Primarily utilized in organic synthesis, this compound serves as a key intermediate in the development of pharmaceuticals and agrochemicals. Its structure, featuring both a carbamate group and an iodine atom, makes it a versatile building block for constructing more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to introduce the pyridine moiety into target compounds. Additionally, the methoxy group enhances its reactivity in various chemical transformations, enabling the synthesis of biologically active molecules. Its applications are particularly significant in the preparation of drug candidates targeting neurological disorders and cancer therapies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,926.00
inventory 250mg
10-20 days ฿4,788.00
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tert-Butyl (4-iodo-2-methoxypyridin-3-yl)carbamate
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Primarily utilized in organic synthesis, this compound serves as a key intermediate in the development of pharmaceuticals and agrochemicals. Its structure, featuring both a carbamate group and an iodine atom, makes it a versatile building block for constructing more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to introduce the pyridine moiety into target compounds. Additionally, the methoxy group enhances its reactivity in various chemical

Primarily utilized in organic synthesis, this compound serves as a key intermediate in the development of pharmaceuticals and agrochemicals. Its structure, featuring both a carbamate group and an iodine atom, makes it a versatile building block for constructing more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to introduce the pyridine moiety into target compounds. Additionally, the methoxy group enhances its reactivity in various chemical transformations, enabling the synthesis of biologically active molecules. Its applications are particularly significant in the preparation of drug candidates targeting neurological disorders and cancer therapies.

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