tert-Butyl (2-fluoro-4-iodopyridin-3-yl)carbamate

Name: tert-Butyl (2-fluoro-4-iodopyridin-3-yl)carbamate
Brand: ChemScene
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CAS No. 1034658-69-9
Cat. No. CS-0372275
Purity≥98%
MDL No.MFCD28401186

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Accessible (Haz class 3, 4, 5 or 8), Domestic	$158.00+
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tert-Butyl (2-fluoro-4-iodopyridin-3-yl)carbamate|CS-0372275

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General Information

CAS No. 1034658-69-9
Cat. No. CS-0372275
Purity ≥98%
MDL No. MFCD28401186
Storage 4°C, protect from light
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₁₀H₁₂FIN₂O₂
Molecular Weight 338.12
Synonym(s) Carbamic acid, N-(2-fluoro-4-iodo-3-pyridinyl)-, 1,1-dimethylethyl ester
SMILES O=C(OC(C)(C)C)NC1=C(I)C=CN=C1F

Description

tert-Butyl (2-fluoro-4-iodopyridin-3-yl)carbamate delivers a fluorinated, iodinated pyridine scaffold with enhanced stability and solubility. This bench-stable building block integrates readily into cross-coupling reactions, enabling efficient access to complex heterocyclic architectures in medicinal chemistry and materials science.

Application

tert-Butyl (2-fluoro-4-iodopyridin-3-yl)carbamate serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its stable iodine handle. The molecule features orthogonal functional groups—fluorine for electrophilic substitution and the Boc-protected amine for selective derivatization—facilitating modular synthesis of complex pyridine-based scaffolds. Its bench stability and ease of purification make it well-suited for high-throughput screening and process-scale applications.

Safety Information

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Computational Chemistry Data

TPSA 51.22
LogP 3.1723
H_Acceptors 3
H_Donors 1
Rotatable_Bonds 1

Other Classifications

Building Blocks Functional Group Amine

Building Blocks Functional Group Iodide

Building Blocks Functional Group Fluoride

Building Blocks Skeleton Aromatic heterocycle compounds Pyridine compounds

Key Words

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tert-Butyl (2-fluoro-4-iodopyridin-3-yl)carbamate

CAS No. 1034658-69-9

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