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m-Iodobenzylchloride

Product Name
m-Iodobenzylchloride
CAS No.
60076-09-7
Chemical Name
m-Iodobenzylchloride
Synonyms
3-iodobenzylchloride;m-Iodobenzylchloride;1-(ChloroMethyl)-3-iodobenzene;Benzene, 1-(chloromethyl)-3-iodo-
CBNumber
CB81454929
Molecular Formula
C7H6ClI
Formula Weight
252.48
MOL File
60076-09-7.mol
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m-Iodobenzylchloride Property

storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
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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

H332Harmful if inhaled

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

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

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
C587950
Product name
1-(Chloromethyl)-3-iodobenzene
Packaging
100mg
Price
$60
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0362310
Product name
1-(CHLOROMETHYL)-3-IODOBENZENE
Purity
95.00%
Packaging
5MG
Price
$504.8
Updated
2021/12/16
AK Scientific
Product number
8955AB
Product name
1-(Chloromethyl)-3-iodobenzene
Packaging
250mg
Price
$136
Updated
2021/12/16
AK Scientific
Product number
8955AB
Product name
1-(Chloromethyl)-3-iodobenzene
Packaging
25g
Price
$586
Updated
2021/12/16
Alichem
Product number
60076097
Product name
3-Iodobenzylchloride
Packaging
500mg
Price
$806.85
Updated
2021/12/16
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m-Iodobenzylchloride Chemical Properties,Usage,Production

Synthesis

57455-06-8

60076-09-7

General procedure for the synthesis of 1-(chloromethyl)-3-iodobenzene from 3-iodobenzyl alcohol: 3-iodobenzyl alcohol (600 mg, 2.56 mmol) was dissolved in dichloromethane (DCM, 3 mL), and thionyl chloride (3 mL, 41.3 mmol) was added, and the reaction was stirred for 18 hours at room temperature. Subsequently, thionyl chloride (1 mL, 13.7 mmol) was added and the reaction mixture was heated to reflux for 12 hours. Upon completion of the reaction, the cooled solution was alkalized with 50% sodium hydroxide solution, diluted with water and extracted with dichloromethane. The organic phases were combined, dried with anhydrous magnesium sulfate, filtered and concentrated to give a clarified slurry. After standing, the slurry crystallized to give 3-iodobenzyl chloride as a white solid (650 mg, quantitative yield).

References

[1] Patent: WO2011/86085, 2011, A1. Location in patent: Page/Page column 39-40
[2] Recueil des Travaux Chimiques des Pays-Bas, 1923, vol. 42, p. 522
[3] Patent: EP1386913, 2004, A1. Location in patent: Page 94
[4] Patent: WO2017/72021, 2017, A1. Location in patent: Page/Page column 76

m-Iodobenzylchloride Preparation Products And Raw materials

Raw materials

Preparation Products

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60076-09-7, m-IodobenzylchlorideRelated Search:


  • m-Iodobenzylchloride
  • 3-iodobenzylchloride
  • 1-(ChloroMethyl)-3-iodobenzene
  • Benzene, 1-(chloromethyl)-3-iodo-
  • 60076-09-7