Basic information Safety Supplier Related

Methyl 4-amino-3-iodobenzoate

Basic information Safety Supplier Related

Methyl 4-amino-3-iodobenzoate Basic information

Product Name:
Methyl 4-amino-3-iodobenzoate
Synonyms:
  • Methyl 4-amino-3-iodobenzozte
  • METHYL 4-AMINO-3-IODOBENZOATE
  • Methyl 4-amino-3-
  • 2-Iodo-4-carboMethoxyaniline
  • Methyl 4-aMino-3-iodobenzoate
  • Methyl 4-aMino-3-iodobenzoate 95% (GC)
  • Methyle4-amino-3-iodobenzoate
  • Benzoic acid, 4-amino-3-iodo-, methyl ester
CAS:
19718-49-1
MF:
C8H8INO2
MW:
277.06
Product Categories:
  • Building Blocks
  • C8 to C9
  • Carbonyl Compounds
  • Chemical Synthesis
  • Organic Building Blocks
  • API intermediates
  • C8 to C9
  • Carbonyl Compounds
  • Esters
  • Aromatic Esters
Mol File:
19718-49-1.mol
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Methyl 4-amino-3-iodobenzoate Chemical Properties

Melting point:
86-91 °C (lit.)
Boiling point:
369.6±32.0 °C(Predicted)
Density 
1.826±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
0.41±0.10(Predicted)
form 
Crystalline Powder
color 
Beige
InChI
InChI=1S/C8H8INO2/c1-12-8(11)5-2-3-7(10)6(9)4-5/h2-4H,10H2,1H3
InChIKey
MRLVFVTVXSKAMX-UHFFFAOYSA-N
SMILES
C(OC)(=O)C1=CC=C(N)C(I)=C1
CAS DataBase Reference
19718-49-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
29224985

MSDS

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Methyl 4-amino-3-iodobenzoate Usage And Synthesis

Definition

ChEBI: Methyl 4-amino-3-iodobenzoate is a benzoate ester.

Synthesis

619-45-4

19718-49-1

General procedure for the synthesis of methyl 4-amino-3-iodobenzoate from methyl 4-aminobenzoate: dissolve methyl 4-aminobenzoate (5.0 g, 0.033 mol), benzyltrimethylammonium dichloroiodonate (22.1 g, 0.056 mol), and calcium carbonate (5.0 g, 0.050 mol) in a solvent mixture of dichloromethane (200 ml) and methanol (100 g). . The reaction mixture was heated to reflux overnight with stirring. Upon completion of the reaction, the solution was cooled to room temperature, washed with saturated sodium bisulfate solution, and the organic phase was dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford the crude product methyl 4-amino-3-iodobenzoate (9.6 g, quantitative yield), which was used in the subsequent reaction without further purification. The structure of the product was confirmed by 1H NMR (400 MHz, DMSO-d6): δ 3.75 (s, 3H), 6.09 (s, 2H), 6.75 (d, J = 8.59 Hz, 1H), 7.66 (dd, J = 8.59, 2.02 Hz, 1H), 8.11 (d, J = 2.02 Hz, 1H).

References

[1] Patent: WO2007/38331, 2007, A2. Location in patent: Page/Page column 30-31
[2] Patent: WO2007/103759, 2007, A2. Location in patent: Page/Page column 48
[3] European Journal of Medicinal Chemistry, 2019, p. 234 - 248
[4] European Journal of Organic Chemistry, 2001, # 24, p. 4607 - 4613
[5] Synlett, 2014, vol. 25, # 3, p. 399 - 402

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