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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
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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
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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.

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N-Bromosuccinimide Price

TRC
Product number
A612705
Product name
6-Amino-5-iodonicotinonitrile
Packaging
50mg
Price
$45
Updated
2021/12/16
TRC
Product number
A612705
Product name
6-Amino-5-iodonicotinonitrile
Packaging
100mg
Price
$90
Updated
2021/12/16
Matrix Scientific
Product number
085104
Product name
6-Amino-5-iodonicotinonitrile
Purity
97%
Packaging
500mg
Price
$188
Updated
2021/12/16
Matrix Scientific
Product number
085104
Product name
6-Amino-5-iodonicotinonitrile
Purity
97%
Packaging
1g
Price
$289
Updated
2021/12/16
AK Scientific
Product number
0656AD
Product name
6-Amino-5-iodonicotinonitrile
Packaging
5g
Price
$691
Updated
2021/12/16
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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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1187322-51-5, 6-Amino-5-iodonicotinonitrileRelated Search:


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