ChemicalBook > CAS DataBase List > 5-FLUORO-2-IODOBENZYL ALCOHOL

5-FLUORO-2-IODOBENZYL ALCOHOL

Product Name
5-FLUORO-2-IODOBENZYL ALCOHOL
CAS No.
877264-43-2
Chemical Name
5-FLUORO-2-IODOBENZYL ALCOHOL
Synonyms
(5-Fluoro-2-iodophenyl);(5-fluoro-2-iodophenyl)methano;5-Fluoro-2-iodobenzylalcohol97%;(5-Fluoro-2-iodophenyl)Methanol;Benzenemethanol, 5-fluoro-2-iodo-;5-Fluoro-2-iodobenzyl alcohol 97%
CBNumber
CB12567317
Molecular Formula
C7H6FIO
Formula Weight
252.02
MOL File
877264-43-2.mol
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5-FLUORO-2-IODOBENZYL ALCOHOL Property

storage temp. 
2-8°C(protect from light)
Appearance
White to off-white Solid
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Safety

HS Code 
2906290090
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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.

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N-Bromosuccinimide Price

Apolloscientific
Product number
PC48326
Product name
5-Fluoro-2-iodobenzylalcohol
Purity
97%
Packaging
250mg
Price
$73
Updated
2021/12/16
SynQuest Laboratories
Product number
2701-K-02
Product name
5-Fluoro-2-iodobenzyl alcohol
Purity
97%
Packaging
250mg
Price
$80
Updated
2021/12/16
Apolloscientific
Product number
PC48326
Product name
5-Fluoro-2-iodobenzylalcohol
Purity
97%
Packaging
1g
Price
$218
Updated
2021/12/16
SynQuest Laboratories
Product number
2701-K-02
Product name
5-Fluoro-2-iodobenzyl alcohol
Purity
97%
Packaging
1g
Price
$240
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0367394
Product name
(5-FLUORO-2-IODOPHENYL)METHANOL
Purity
95.00%
Packaging
5MG
Price
$496.72
Updated
2021/12/16
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5-FLUORO-2-IODOBENZYL ALCOHOL Chemical Properties,Usage,Production

Synthesis

52548-63-7

877264-43-2

Step 1: 5-fluoro-2-iodobenzoic acid (5.00 g, 18.80 mmol) was dissolved in tetrahydrofuran (50 mL) and cooled to 0 °C under nitrogen protection. The borane-dimethyl sulfide complex (3.57 mL, 37.60 mmol) was slowly added dropwise under stirring conditions, followed by gradual warming of the reaction mixture to room temperature. The reaction was stirred continuously for 16 hours at room temperature. Upon completion of the reaction, the mixture was carefully poured into ice and quenched by adding 10% aqueous potassium carbonate solution (50 mL). The mixture was extracted with dichloromethane (2 x 50 mL), the organic phases were combined, dried over magnesium sulfate and subsequently concentrated under reduced pressure to give 5-fluoro-2-iodobenzyl alcohol as a colorless solid (4.80 g, 91% yield).1H NMR (400 MHz, CDCl3): δ 7.68 (dd, 1H, J= Hz), 7.19 (dd, 1H, J= Hz), and 6.70 (td, 1H, J= Hz), 4.57 (d, 2H, J= Hz), 1.95 (t, 1H, J= Hz).

References

[1] Advanced Synthesis and Catalysis, 2015, vol. 357, # 14-15, p. 3206 - 3214
[2] Organic Letters, 2018, vol. 20, # 2, p. 345 - 348
[3] Patent: WO2013/132376, 2013, A1. Location in patent: Page/Page column 238
[4] Patent: US2006/52378, 2006, A1. Location in patent: Page/Page column 146
[5] Chemical Communications, 2013, vol. 49, # 31, p. 3254 - 3256

5-FLUORO-2-IODOBENZYL ALCOHOL Preparation Products And Raw materials

Raw materials

Preparation Products

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5-FLUORO-2-IODOBENZYL ALCOHOL Suppliers

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877264-43-2, 5-FLUORO-2-IODOBENZYL ALCOHOLRelated Search:


  • (5-Fluoro-2-iodophenyl)Methanol
  • 5-Fluoro-2-iodobenzyl alcohol 97%
  • (5-fluoro-2-iodophenyl)methano
  • 5-Fluoro-2-iodobenzylalcohol97%
  • (5-Fluoro-2-iodophenyl)
  • Benzenemethanol, 5-fluoro-2-iodo-
  • 877264-43-2