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9-iodoanthracene

Product Name
9-iodoanthracene
CAS No.
22362-86-3
Chemical Name
9-iodoanthracene
Synonyms
9-iodoanthracene;Anthracene, 9-iodo-
CBNumber
CB02548119
Molecular Formula
C14H9I
Formula Weight
304.13
MOL File
22362-86-3.mol
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9-iodoanthracene Property

Melting point:
82-83 °C
Boiling point:
411.0±14.0 °C(Predicted)
Density 
1.692±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Matrix Scientific
Product number
096747
Product name
9-Iodoanthracene
Purity
95+%
Packaging
250mg
Price
$364
Updated
2021/12/16
Matrix Scientific
Product number
096747
Product name
9-Iodoanthracene
Purity
95+%
Packaging
1g
Price
$807
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0136343
Product name
9-IODOANTHRACENE
Purity
95.00%
Packaging
1G
Price
$1039.5
Updated
2021/12/16
Crysdot
Product number
CD41001558
Product name
9-Iodoanthracene
Purity
95+%
Packaging
1g
Price
$320
Updated
2021/12/16
Crysdot
Product number
CD41001558
Product name
9-Iodoanthracene
Purity
95+%
Packaging
5g
Price
$960
Updated
2021/12/16
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9-iodoanthracene Chemical Properties,Usage,Production

Synthesis

1564-64-3

22362-86-3

Under argon protection, 6 g (23.33 mmol) of 9-bromoanthracene was placed in a 250 mL two-necked round-bottomed flask and dissolved by adding 100 mL of anhydrous tetrahydrofuran. At -78 °C, 14.58 mL of 2.4 M (35 mmol) n-butyllithium solution was slowly added dropwise, and the dropwise process was completed in about 30 min. After the dropwise addition was completed, the reaction mixture was kept at -78 °C to -50 °C for 2 hours. Subsequently, 10.7 g (42 mmol) of iodine was added and slowly warmed to room temperature after 45 minutes. The reaction mixture was continued to be magnetically stirred at room temperature for about 12 hours. Upon completion of the reaction, the reaction was quenched with a small amount of sodium bisulfite solution and stirred for 30 minutes. The reaction solution was extracted with dichloromethane and the organic layer was separated. The organic phase was dried with anhydrous magnesium sulfate, filtered and concentrated until a small amount of solvent remained. Anhydrous methanol was added to precipitate the yellow solid 9-iodoanthracene. The final product was obtained as 4.1 g in 56.55% yield.

References

[1] Journal of the American Chemical Society, 2010, vol. 132, # 47, p. 16759 - 16761
[2] Synthesis, 1986, # 1, p. 121 - 122
[3] Organic Letters, 2010, vol. 12, # 13, p. 3050 - 3053
[4] European Journal of Organic Chemistry, 2011, # 3, p. 478 - 496
[5] Patent: CN104163824, 2017, B. Location in patent: Paragraph 0037; 0038

9-iodoanthracene Preparation Products And Raw materials

Raw materials

Preparation Products

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9-iodoanthracene Suppliers

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22362-86-3, 9-iodoanthraceneRelated Search:


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