Methyl 4-amino-3-iodobenzoate

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CAS:19718-49-1
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CAS:19718-49-1
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Products Intro: Product Name:Methyl 4-amino-3-iodobenzoate
CAS:19718-49-1
Purity:0.98 Package:1KG;10KG;50KG

Methyl 4-amino-3-iodobenzoate manufacturers

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
EINECS:
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
Methyl 4-amino-3-iodobenzoate Structure
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
pka0.41±0.10(Predicted)
form Crystalline Powder
color Beige
InChIInChI=1S/C8H8INO2/c1-12-8(11)5-2-3-7(10)6(9)4-5/h2-4H,10H2,1H3
InChIKeyMRLVFVTVXSKAMX-UHFFFAOYSA-N
SMILESC(OC)(=O)C1=CC=C(N)C(I)=C1
CAS DataBase Reference19718-49-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
HS Code 29224985
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
Methyl 4-amino-3-iodobenzoate Usage And Synthesis
DefinitionChEBI: Methyl 4-amino-3-iodobenzoate is a benzoate ester.
Synthesis
Methyl 4-aminobenzoate

619-45-4

Methyl 4-amino-3-iodobenzoate

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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