ChemicalBook > CAS DataBase List > Methyl 4-amino-5-iodo-2-methylbenzoate

Methyl 4-amino-5-iodo-2-methylbenzoate

Product Name
Methyl 4-amino-5-iodo-2-methylbenzoate
CAS No.
672293-33-3
Chemical Name
Methyl 4-amino-5-iodo-2-methylbenzoate
Synonyms
187484;Methyl 4-amino-5-iodo-2-methylbenzoate;4-Amino-5-iodo-2-methyl-benzoic acid methyl ester;Benzoic acid, 4-amino-5-iodo-2-methyl-, methyl ester
CBNumber
CB22534945
Molecular Formula
C9H10INO2
Formula Weight
291.09
MOL File
672293-33-3.mol
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Methyl 4-amino-5-iodo-2-methylbenzoate Property

Boiling point:
367.0±42.0 °C(Predicted)
Density 
1.733±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
0.53±0.10(Predicted)
Appearance
Light yellow to yellow Solid
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

AK Scientific
Product number
4724DF
Product name
Methyl4-amino-5-iodo-2-methylbenzoate
Packaging
1g
Price
$251
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0037325
Product name
METHYL 4-AMINO-5-IODO-2-METHYLBENZOATE
Purity
95.00%
Packaging
5G
Price
$909.56
Updated
2021/12/16
Ambeed
Product number
A248886
Product name
Methyl4-amino-5-iodo-2-methylbenzoate
Purity
97%
Packaging
100mg
Price
$32
Updated
2021/12/16
Ambeed
Product number
A248886
Product name
Methyl4-amino-5-iodo-2-methylbenzoate
Purity
97%
Packaging
250mg
Price
$62
Updated
2021/12/16
Ambeed
Product number
A248886
Product name
Methyl4-amino-5-iodo-2-methylbenzoate
Purity
97%
Packaging
1g
Price
$163
Updated
2021/12/16
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Methyl 4-amino-5-iodo-2-methylbenzoate Chemical Properties,Usage,Production

Synthesis

6933-47-7

672293-33-3

Methyl 2-methyl-4-aminobenzoate (Intermediate 7) (2.9 g, 16.6 mmol) was used as raw material and dissolved in DMF (15 ml), sodium periodate (1.45 g, 6.6 mmol) and iodine (3.4 g, 13.3 mmol) were added sequentially. The reaction mixture was stirred at a constant temperature at 50°C for 2 hours. After the reaction was completed, the mixture was slowly poured into cold water containing NaHSO3 (0.5 g). After stirring and mixing, the mixture was allowed to stand overnight. On the following day, the precipitate was collected by filtration, washed with water and subsequently dissolved with dichloromethane. The resulting solution was dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure to afford the target product methyl 4-amino-5-iodo-2-methylbenzoate as an orange solid (4.1 g, 85% yield). The structure of the product was confirmed by 1H NMR (300 MHz, CDCl3): δ 8.20 (s, 1H), 6.47 (s, 1H), 3.75 (s, 3H), 2.42 (s, 3H).

References

[1] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 3, p. 942 - 945
[2] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 3, p. 946 - 949
[3] Patent: WO2009/47240, 2009, A1. Location in patent: Page/Page column 30
[4] Patent: US2018/291002, 2018, A1. Location in patent: Paragraph 0462; 0463
[5] Patent: US2004/142940, 2004, A1. Location in patent: Page/Page column 42

Methyl 4-amino-5-iodo-2-methylbenzoate Preparation Products And Raw materials

Raw materials

Preparation Products

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Methyl 4-amino-5-iodo-2-methylbenzoate Suppliers

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672293-33-3, Methyl 4-amino-5-iodo-2-methylbenzoateRelated Search:


  • Methyl 4-amino-5-iodo-2-methylbenzoate
  • 4-Amino-5-iodo-2-methyl-benzoic acid methyl ester
  • 187484
  • Benzoic acid, 4-amino-5-iodo-2-methyl-, methyl ester
  • 672293-33-3