Tert-butyl (4-hydroxy-3-iodophenethyl)carbamate

97%

Reagent Code: #238446
label
Alias tert-Butyl 4-hydroxy-3-iodophenethylcarbamate; N-tert-Butoxycarbonyl 3-Iodotyramine; [2-(4-Hydroxy-3-iodophenyl)ethyl]carbaMicAcid1,1-DiMethylethylEster; N-(tert-Butoxycarbonyl)[2-(4-hydroxy-3-iodophenyl)ethyl]aMine;tert-Butyl4Chemicalbook-hydroxy-3-iodop
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CAS Number 788824-50-0
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Properties Soluble in chloroform (a little), ethyl acetate (a little), methanol (a little)

science Other reagents with same CAS 788824-50-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 363.19 g/mol
Formula C₁₃H₁₈INO₃
badge Registry Numbers
MDL Number MFCD07779453
thermostat Physical Properties
Melting Point 129-130 °C
Boiling Point 412.0±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.528±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of radiolabeled agents for medical imaging. The iodine moiety allows for incorporation of radioactive isotopes such as iodine-123 or iodine-131, making it valuable in creating tracers for single-photon emission computed tomography (SPECT). Its protected amine group facilitates selective reactions in multi-step organic syntheses, especially in the preparation of bioactive molecules targeting neurological and endocrine systems. Also employed in the production of specialty reagents for research in receptor binding and metabolic pathways.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿7,050.00
inventory 1g
10-20 days ฿30,720.00
inventory 5g
10-20 days ฿122,860.00
inventory 250mg
10-20 days ฿14,750.00
Tert-butyl (4-hydroxy-3-iodophenethyl)carbamate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of radiolabeled agents for medical imaging. The iodine moiety allows for incorporation of radioactive isotopes such as iodine-123 or iodine-131, making it valuable in creating tracers for single-photon emission computed tomography (SPECT). Its protected amine group facilitates selective reactions in multi-step organic syntheses, especially in the preparation of bioactive molecules targeting neurological

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of radiolabeled agents for medical imaging. The iodine moiety allows for incorporation of radioactive isotopes such as iodine-123 or iodine-131, making it valuable in creating tracers for single-photon emission computed tomography (SPECT). Its protected amine group facilitates selective reactions in multi-step organic syntheses, especially in the preparation of bioactive molecules targeting neurological and endocrine systems. Also employed in the production of specialty reagents for research in receptor binding and metabolic pathways.

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