6-IODO-PYRIDIN-2-YLAMINE
- Product Name
- 6-IODO-PYRIDIN-2-YLAMINE
- CAS No.
- 88511-25-5
- Chemical Name
- 6-IODO-PYRIDIN-2-YLAMINE
- Synonyms
- 6-iodopyridin-2-aMine;6-iodo-2-pyridinamine;2-AMino-6-iodopyridine;2-PyridinaMine, 6-iodo-;6-Iodo-pyridine-2ylamine;6-IODO-PYRIDIN-2-YLAMINE
- CBNumber
- CB5765197
- Molecular Formula
- C5H5IN2
- Formula Weight
- 220.01
- MOL File
- 88511-25-5.mol
6-IODO-PYRIDIN-2-YLAMINE Property
- Melting point:
- 103-104°C
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- form
- solid
- Appearance
- White to light yellow Solid
Safety
- Hazard Codes
- Xi
- HazardClass
- IRRITANT
- HS Code
- 2933399990
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- ADE000340
- Product name
- 6-Iodo-pyridin-2-ylamine
- Purity
- AldrichCPR
- Packaging
- 1g
- Price
- $497
- Updated
- 2025/07/31
- Product number
- B450615
- Product name
- 6-iodopyridin-2-amine
- Packaging
- 100mg
- Price
- $155
- Updated
- 2021/12/16
- Product number
- OR913273
- Product name
- 6-Iodopyridin-2-amine
- Purity
- 95%
- Packaging
- 250mg
- Price
- $55
- Updated
- 2021/12/16
- Product number
- 3H30-H-0G
- Product name
- 6-Iodopyridin-2-amine
- Purity
- 95%
- Packaging
- 250mg
- Price
- $88
- Updated
- 2021/12/16
- Product number
- 023722
- Product name
- 6-Iodo-pyridin-2-ylamine
- Purity
- 98%
- Packaging
- 250mg
- Price
- $125
- Updated
- 2021/12/16
6-IODO-PYRIDIN-2-YLAMINE Chemical Properties,Usage,Production
Synthesis
19798-81-3
88511-25-5
General procedure for the synthesis of 6-iodopyridin-2-amine from 2-amino-6-bromopyridine: 2-bromo-6-aminopyridine (519 mg), cuprous iodide (29 mg), sodium iodide (899 mg), and N,N-dimethylethylenediamine (26 mg) were dissolved in dioxane (5 mL) and heated to react for 6 hours at 110 °C in an inert atmosphere. Upon completion of the reaction, concentrated ammonia (8 mL) was added, followed by water (10 mL). The reaction mixture was extracted with dichloromethane (3 x 15 mL) and the organic phase was dried with anhydrous magnesium sulfate, filtered and concentrated. The crude product was purified by rapid chromatography on silica gel using a 0-10% methanol/dichloromethane gradient elution to afford 6-iodopyridin-2-amine as a beige solid (530 mg, 80% yield). The structure of the product was confirmed by 1H NMR (CDCl3): δ 4.60 (s, 2H), 6.41-6.44 (m, 1H), 7.00-7.08 (m, 2H); mass spectrometry (MS) showed the molecular ion peak m/z 221 (MH+).
References
[1] RSC Advances, 2013, vol. 3, # 26, p. 10296 - 10300
[2] Patent: WO2005/60970, 2005, A1. Location in patent: Page/Page column 117
6-IODO-PYRIDIN-2-YLAMINE Preparation Products And Raw materials
Raw materials
Preparation Products
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