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Methyl 4-iodosalicylate

Basic information Structure Safety Supplier Related

Methyl 4-iodosalicylate Basic information

Product Name:
Methyl 4-iodosalicylate
Synonyms:
  • Methyl 2-Hydroxy-4-iodobenzoate 4-Iodosalicylic Acid Methyl Ester 2-Hydroxy-4-iodobenzoic Acid Methyl Ester
  • Methyl 4-iodosalicylate, 5-Iodo-2-(methoxycarbonyl)phenol
  • Methyl 4-iodosalicylate 97%
  • Methyl4-Iodosilicylate
  • 2-Hydroxy-4-iodobenzoic Acid Methyl Ester
  • 4-Iodosalicylic Acid Methyl Ester
  • Methyl4-Iodosalicylate>
  • Benzoic acid, 2-hydroxy-4-iodo-, methyl ester
CAS:
18179-39-0
MF:
C8H7IO3
MW:
278.04
Mol File:
18179-39-0.mol
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Methyl 4-iodosalicylate Chemical Properties

Melting point:
69-73 °C
Boiling point:
309.7±32.0 °C(Predicted)
Density 
1.880±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
Chloroform (Slightly), Methanol (Slightly)
form 
powder to crystal
pka
8.91±0.10(Predicted)
color 
White to Gray to Brown
Sensitive 
Light Sensitive
InChIKey
WUFUURSWOJROKY-UHFFFAOYSA-N
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Safety Information

Hazard Codes 
T
Risk Statements 
25
Safety Statements 
45
RIDADR 
UN 2811 6.1/PG 3
WGK Germany 
3
8
Hazard Note 
Toxic
PackingGroup 
III
HS Code 
2918290090
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Methyl 4-iodosalicylate Usage And Synthesis

Structure

2-hy­droxy-4-iodo­benzoic acid methyl ester (methyl 4-iodo­salicylate, C8H7IO3) allows for an effective way of incorporating the methyl salicylates within larger organic mol­ecules, using such methodologies as McClure protocols, which take advantage of the iodine atom at the 4-position of the aromatic ring for the formation of carbon-carbon bonds. The iodine atom is also capable of forming supra­molecular synthons, which may be useful for crystal engineering. At 90 K, the methyl 4-iodo­salicylat displays monoclinic (P21/c) symmetry with one mol­ecule in the asymmetric unit. Inter­molecular hydrogen bonding inter­actions occur between the hy­droxy groups of one mol­ecule and the carbonyl oxygen atom of the methyl ester of an adjacent mol­ecule to form a centrosymmetric dimeric pair with H⋯O = 2.53 (4) Å. An O3—H3⋯O2 intra­molecular hydrogen bond also exists with an H⋯O distance of 2.05 (4) Å. The C5⋯C8 [3.326 (3) Å] and O3⋯H1C (2.51 Å) inter­actions provide only short contacts between the stacks of offset (102) parallel sheets, which make up the crystal. These sheets, in turn, contain the inversion-generated hydrogen-bonded dimers. The non-hydrogen atoms of the mol­ecule are essentially coplanar with no displacement from the mean mol­ecular plane greater than 0.132 Å.

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