6-Amino-5-iodonicotinonitrile
- Product Name
- 6-Amino-5-iodonicotinonitrile
- CAS No.
- 1187322-51-5
- Chemical Name
- 6-Amino-5-iodonicotinonitrile
- Synonyms
- 6-Amino-5-iodonicotinonitrile;6-amino-5-iodo-3-pyridinecarbonitrile;3-Pyridinecarbonitrile, 6-amino-5-iodo-
- CBNumber
- CB42691758
- Molecular Formula
- C6H4IN3
- Formula Weight
- 245.02
- MOL File
- 1187322-51-5.mol
6-Amino-5-iodonicotinonitrile Property
- Boiling point:
- 343.8±42.0 °C(Predicted)
- Density
- 2.11±0.1 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2–8 °C
- pka
- 1.08±0.49(Predicted)
- Appearance
- Light yellow to yellow Solid
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
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
- A612705
- Product name
- 6-Amino-5-iodonicotinonitrile
- Packaging
- 50mg
- Price
- $45
- Updated
- 2021/12/16
- Product number
- A612705
- Product name
- 6-Amino-5-iodonicotinonitrile
- Packaging
- 100mg
- Price
- $90
- Updated
- 2021/12/16
- Product number
- 085104
- Product name
- 6-Amino-5-iodonicotinonitrile
- Purity
- 97%
- Packaging
- 500mg
- Price
- $188
- Updated
- 2021/12/16
- Product number
- 085104
- Product name
- 6-Amino-5-iodonicotinonitrile
- Purity
- 97%
- Packaging
- 1g
- Price
- $289
- Updated
- 2021/12/16
- Product number
- 0656AD
- Product name
- 6-Amino-5-iodonicotinonitrile
- Packaging
- 5g
- Price
- $691
- Updated
- 2021/12/16
6-Amino-5-iodonicotinonitrile Chemical Properties,Usage,Production
Synthesis
4214-73-7
1187322-51-5
Synthesis of 6-amino-5-iodonicotinonitrile: 6-amino-3-pyridinecarbonitrile (10.0 g, 0.081 mol), silver trifluoroacetate (25.5 g, 0.115 mol) and 1,2-dichloroethane (160 mL) were added to a flask and heated and refluxed for 5 hours. Iodine (29.5 g, 0.116 mol) was then added and heating and refluxing was continued for 18 hours. Upon completion of the reaction, the mixture was cooled, filtered, and partitioned between water and 1,2-dichloroethane. The organic and aqueous phases were filtered through diatomaceous earth, respectively. The aqueous phase was extracted repeatedly with 1,2-dichloroethane until depleted, the organic phases were combined, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was dissolved in ethyl acetate and washed with sodium thiosulfate solution. The solvent was removed under reduced pressure to give 6.6 g of pale yellow crystalline product, which could be used in the next reaction without further purification.HPLC retention time: 2.57 min; LCMS (m/z): 246 [M + H]+.
References
[1] Journal of Medicinal Chemistry, 2013, vol. 56, # 3, p. 1160 - 1170
[2] Patent: US2015/218155, 2015, A1. Location in patent: Paragraph 0300
[3] Patent: WO2009/112139, 2009, A1. Location in patent: Page/Page column 25
6-Amino-5-iodonicotinonitrile Preparation Products And Raw materials
Raw materials
Preparation Products
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