N-Cbz-4-iodoaniline

95%

Reagent Code: #36947
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CAS Number 93298-14-7

science Other reagents with same CAS 93298-14-7

blur_circular Chemical Specifications

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Weight 353.1551 g/mol
Formula C₁₄H₁₂INO₂
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MDL Number MFCD00745576
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive compounds. The Cbz (carbobenzyloxy) group serves as a protecting group for the amine functionality, allowing selective manipulation of other sites, such as the iodine substituent. It acts as a precursor in the synthesis of complex molecules with potential therapeutic applications, owing to the reactivity of the iodine in cross-coupling reactions like Suzuki coupling or Buchwald-Hartwig amination. Its versatility makes it valuable in medicinal chemistry and drug discovery research.

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inventory 100mg
10-20 days ฿1,728.00

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N-Cbz-4-iodoaniline
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive compounds. The Cbz (carbobenzyloxy) group serves as a protecting group for the amine functionality, allowing selective manipulation of other sites, such as the iodine substituent. It acts as a precursor in the synthesis of complex molecules with potential therapeutic applications, owing to the reactivity of the iodine in cross-coupling reactions like Suzuki coupling or Buchwald-Hartwig amination

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive compounds. The Cbz (carbobenzyloxy) group serves as a protecting group for the amine functionality, allowing selective manipulation of other sites, such as the iodine substituent. It acts as a precursor in the synthesis of complex molecules with potential therapeutic applications, owing to the reactivity of the iodine in cross-coupling reactions like Suzuki coupling or Buchwald-Hartwig amination. Its versatility makes it valuable in medicinal chemistry and drug discovery research.

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