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Merck
CN

552453

2-氟-5-碘苯甲腈

97%

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线性分子式:
C6H3FICN
化学文摘社编号:
分子量:
247.01
UNSPSC Code:
12352100
PubChem Substance ID:
MDL number:
Assay:
97%
Form:
solid
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assay

97%

form

solid

mp

72-76 °C (lit.)

SMILES string

Fc1ccc(I)cc1C#N

InChI

1S/C7H3FIN/c8-7-2-1-6(9)3-5(7)4-10/h1-3H

InChI key

BIZHQRAAZMDWNK-UHFFFAOYSA-N

General description

2-Fluoro-5-iodobenzonitrile is a halogenated benzonitrile. It participates in the preparation of 4-phenoxy benzamide riboside, a key intermediate formed during the chemical synthesis of 4-phenoxybenzamide adenine dinucleotide.

Application

2-Fluoro-5-iodobenzonitrile may be used in the synthesis of 5-substituted-3-amino indazoles and 5-iodo-1-methyl-1H-indazol-3-amine.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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分析证书(COA)

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Scaffold oriented synthesis. Part 3: design, synthesis and biological evaluation of novel 5-substituted indazoles as potent and selective kinase inhibitors employing [2+ 3] cycloadditions.
Akritopoulou-Zanze I, et al.
Bioorganic & Medicinal Chemistry Letters, 21(5), 1476-1479 (2011)
Synthesis of 4-phenoxybenzamide adenine dinucleotide as NAD analogue with inhibitory activity against enoyl-ACP reductase (InhA) of Mycobacterium tuberculosis.
Bonnac L, et al.
Bioorganic & Medicinal Chemistry Letters, 17(16), 4588-4591 (2007)
A method for the regioselective synthesis of 1-alkyl-1H-indazoles.
Liu HJ, et al.
Tetrahedron, 69(19), 3907-3912 (2013)

全球贸易项目编号

货号GTIN
552453-5G04061832100883

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