ChemicalBook > CAS DataBase List > BENZOIC ACID, 2-AMINO-4-CHLORO-5-IODO-, METHYL ESTER

BENZOIC ACID, 2-AMINO-4-CHLORO-5-IODO-, METHYL ESTER

Product Name
BENZOIC ACID, 2-AMINO-4-CHLORO-5-IODO-, METHYL ESTER
CAS No.
199850-56-1
Chemical Name
BENZOIC ACID, 2-AMINO-4-CHLORO-5-IODO-, METHYL ESTER
Synonyms
Methyl 2-aMino-4-chloro-5-iodobenzoate;Methyl 4-chloro-5-iodoanthranilate;2-AMino-4-chloro-5-iodo-benzoic acid Methyl ester;BENZOIC ACID, 2-AMINO-4-CHLORO-5-IODO-, METHYL ESTER
CBNumber
CB52468676
Molecular Formula
C8H7ClINO2
Formula Weight
311.5
MOL File
199850-56-1.mol
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BENZOIC ACID, 2-AMINO-4-CHLORO-5-IODO-, METHYL ESTER Property

Boiling point:
369.2±42.0 °C(Predicted)
Density 
1.903
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
0.99±0.10(Predicted)
Appearance
Off-white to gray Solid
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
M331750
Product name
Methyl2-Amino-4-chloro-5-iodobenzoate
Packaging
100mg
Price
$60
Updated
2021/12/16
AK Scientific
Product number
CS-0041075
Product name
Methyl2-amino-4-chloro-5-iodobenzoate
Packaging
5g
Price
$153
Updated
2021/12/16
Crysdot
Product number
CD12098816
Product name
Methyl2-amino-4-chloro-5-iodobenzoate
Purity
95+%
Packaging
5g
Price
$168
Updated
2021/12/16
Chemenu
Product number
CM155772
Product name
methyl2-amino-4-chloro-5-iodobenzoate
Purity
95%
Packaging
5g
Price
$196
Updated
2021/12/16
Alichem
Product number
199850561
Product name
Methyl2-amino-4-chloro-5-iodobenzoate
Packaging
5g
Price
$224.7
Updated
2021/12/16
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BENZOIC ACID, 2-AMINO-4-CHLORO-5-IODO-, METHYL ESTER Chemical Properties,Usage,Production

Synthesis

5900-58-3

199850-56-1

General procedure for the synthesis of methyl 4-chloro-5-iodo-2-aminobenzoate from methyl 2-amino-4-chlorobenzoate: Methyl 2-amino-4-chlorobenzoate (50 g, 0.27 mol) was added to a solution of anhydrous ethanol (2.5 L) containing iodine (68 g, 0.27 mol) and silver sulfate (84 g, 0.27 mol). The reaction mixture was stirred at room temperature for 45 minutes. Subsequently, the reaction mixture was filtered through a Celite pad to remove insoluble impurities. The filtrate was concentrated under reduced pressure and the residue was dissolved in ethyl acetate (2 L) and washed sequentially with saturated aqueous sodium bicarbonate (3 x 400 mL), water (3 x 400 mL) and brine. The organic phase was dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford the target product methyl 2-amino-4-chloro-5-iodobenzoate (85 g, 99% yield).

References

[1] Journal of Labelled Compounds and Radiopharmaceuticals, 2003, vol. 46, # 10, p. 993 - 1000
[2] Chemical Communications, 2017, vol. 53, # 62, p. 8735 - 8738
[3] Patent: WO2010/65134, 2010, A1. Location in patent: Page/Page column 60-61
[4] Patent: WO2015/54572, 2015, A1. Location in patent: Page/Page column 261; 262
[5] Patent: WO2012/119978, 2012, A1. Location in patent: Page/Page column 50

BENZOIC ACID, 2-AMINO-4-CHLORO-5-IODO-, METHYL ESTER Preparation Products And Raw materials

Raw materials

Preparation Products

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199850-56-1, BENZOIC ACID, 2-AMINO-4-CHLORO-5-IODO-, METHYL ESTERRelated Search:


  • BENZOIC ACID, 2-AMINO-4-CHLORO-5-IODO-, METHYL ESTER
  • Methyl 4-chloro-5-iodoanthranilate
  • 2-AMino-4-chloro-5-iodo-benzoic acid Methyl ester
  • Methyl 2-aMino-4-chloro-5-iodobenzoate
  • 199850-56-1