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2-Bromo-4-iodoanisole

Product Name
2-Bromo-4-iodoanisole
CAS No.
182056-39-9
Chemical Name
2-Bromo-4-iodoanisole
Synonyms
2-Bromo-4-iodoanisole;2-bromo-4-iodobenzene methyl ether;Benzene, 2-bromo-4-iodo-1-methoxy-;2-Bromo-4-iodo-1-methoxybenzene, 2-Bromo-4-iodophenyl methyl ether
CBNumber
CB61568783
Molecular Formula
C7H6BrIO
Formula Weight
312.93
MOL File
182056-39-9.mol
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2-Bromo-4-iodoanisole Property

Melting point:
80-82 °C(Solv: hexane (110-54-3); toluene (108-88-3))
Boiling point:
285.1±30.0 °C(Predicted)
Density 
2.062±0.06 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
form 
crystals
color 
Off white to faint peach
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Safety

HS Code 
2909309090
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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.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

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N-Bromosuccinimide Price

TRC
Product number
B678690
Product name
2-Bromo-4-iodoanisole
Packaging
500mg
Price
$200
Updated
2021/12/16
Apolloscientific
Product number
OR45120
Product name
2-Bromo-4-iodoanisole
Packaging
1g
Price
$47
Updated
2021/12/16
SynQuest Laboratories
Product number
2607-S-X2
Product name
2-Bromo-4-iodoanisole
Packaging
1g
Price
$52
Updated
2021/12/16
AK Scientific
Product number
9539AA
Product name
2-Bromo-4-iodoanisole
Packaging
1g
Price
$67
Updated
2021/12/16
Apolloscientific
Product number
OR45120
Product name
2-Bromo-4-iodoanisole
Packaging
5g
Price
$209
Updated
2021/12/16
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2-Bromo-4-iodoanisole Chemical Properties,Usage,Production

Uses

2-Bromo-4-iodoanisole is an electrophilic intermediate used in organic synthesis.

Preparation

2-Bromo-4-iodoanisole is synthetically prepared by regioselective halogenations of 4-iodoanisole.

Synthesis

578-57-4

182056-39-9

The general procedure for the synthesis of 2-bromo-4-iodo-1-methoxybenzene from 2-bromoanisole was as follows: to a stirred solution of 2-bromoanisole (1 mmol) in dichloromethane (CH2Cl2) or 1,2-dichloroethane ((CH2Cl)2) (0.1 M) was added sequentially Ph3PAuNTf2 (0.025 mmol, 19 mg; if using the 2:1 complex of Ph3PAuNTf2 with toluene) and N-iodosuccinimide (1.1 mmol, 248 mg). The reaction mixture was stirred at room temperature or reacted under reflux conditions until complete conversion of the feedstock was confirmed by thin layer chromatography (TLC) monitoring. Upon completion of the reaction, the solvent was evaporated under reduced pressure and the resulting crude product was purified by fast column chromatography using different gradient elutions of hexane and ethyl acetate (EtOAc) to give pure 2-bromo-4-iodo-1-methoxybenzene.

References

[1] Synlett, 2014, vol. 25, # 3, p. 399 - 402
[2] Synthetic Communications, 2007, vol. 37, # 8, p. 1259 - 1265
[3] Canadian Journal of Chemistry, 2005, vol. 83, # 10, p. 1808 - 1811
[4] Tetrahedron Letters, 2004, vol. 45, # 43, p. 8015 - 8018

2-Bromo-4-iodoanisole Preparation Products And Raw materials

Raw materials

Preparation Products

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2-Bromo-4-iodoanisole Suppliers

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Shijiazhuang Sdyano Fine Chemical Co., Ltd.
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182056-39-9, 2-Bromo-4-iodoanisoleRelated Search:


  • 2-Bromo-4-iodoanisole
  • 2-Bromo-4-iodo-1-methoxybenzene, 2-Bromo-4-iodophenyl methyl ether
  • Benzene, 2-bromo-4-iodo-1-methoxy-
  • 2-bromo-4-iodobenzene methyl ether
  • 182056-39-9
  • Anisoles, Alkyloxy Compounds & Phenylacetates
  • Bromine Compounds
  • Iodine Compounds