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5-BROMO INDOLE-7-CARBOXYLIC ACID METHYL ESTER

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Products Intro: Product Name:Methyl 5-Bromoindole-7-carboxylate
CAS:860624-89-1
Purity:>=97% Package:0.1g;0.25g;1g;5g;10g
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Products Intro: Product Name:Methyl 5-bromoindole-7-carboxylate
CAS:860624-89-1
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-07100
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Products Intro: Product Name:5-BROMO INDOLE-7-CARBOXYLIC ACID METHYL ESTER
CAS:860624-89-1
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Products Intro: Product Name:methyl 5-bromo-1H-indole-7-carboxylate
CAS:860624-89-1
Purity:0.97 Package:1KG;25KG
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Products Intro: Product Name:5-BROMO INDOLE-7-CARBOXYLIC ACID METHYL ESTER
CAS:860624-89-1
Purity:0.98 Package:1g; 5g; 10g; 25g; 100g

5-BROMO INDOLE-7-CARBOXYLIC ACID METHYL ESTER manufacturers

5-BROMO INDOLE-7-CARBOXYLIC ACID METHYL ESTER Basic information
Product Name:5-BROMO INDOLE-7-CARBOXYLIC ACID METHYL ESTER
Synonyms:5-BROMO INDOLE-7-CARBOXYLIC ACID METHYL ESTER;Methyl 5-bromoindole-7-carboxylate;5-BroMo-1H-indol-7-carboxylic acid Methyl ester;1H-Indole-7-carboxylic acid, 5-bromo-, methyl ester;5-Bromo-1H-indole-7-carboxylic acid methyl ester;1H-Indole-7-carboxylic acid, 5-bromo-, methyl ester (9CI, ACI);5-bromo-1H-Indole-7-carboxylic acid methyl ester (9CI ACI);methyl 5-bromo-1H-indole-7-carboxylate
CAS:860624-89-1
MF:C10H8BrNO2
MW:254.08
EINECS:
Product Categories:
Mol File:860624-89-1.mol
5-BROMO INDOLE-7-CARBOXYLIC ACID METHYL ESTER Structure
5-BROMO INDOLE-7-CARBOXYLIC ACID METHYL ESTER Chemical Properties
Boiling point 382.6±22.0 °C(Predicted)
density 1.629±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka14.46±0.30(Predicted)
AppearanceLight yellow to brown Solid
CAS DataBase Reference860624-89-1
Safety Information
MSDS Information
5-BROMO INDOLE-7-CARBOXYLIC ACID METHYL ESTER Usage And Synthesis
Synthesis
5-BROMO INDOLE-7-CARBOXYLIC ACID

860624-90-4

Iodomethane

74-88-4

5-BROMO INDOLE-7-CARBOXYLIC ACID METHYL ESTER

860624-89-1

Iodomethane (7.81 mL, 125 mmol) was slowly added dropwise to a solution of N,N-dimethylformamide (50 mL) containing 5-bromo-1H-indole-7-carboxylic acid (10 g, 41.7 mmol) and sodium carbonate (17.66 g, 167 mmol). The reaction mixture was stirred continuously for 2 h at room temperature. Upon completion of the reaction, it was filtered through a silica gel pad (500 g) and eluted with ether (600 mL). The collected eluate was washed once with deionized water (100 mL) and subsequently concentrated under reduced pressure to afford methyl 5-bromoindole-7-carboxylate (9.65 g, 91% yield). The product was confirmed by LC/MS analysis: m/z 253.8 (M+), retention time 2.15 min.

References[1] Patent: WO2008/118724, 2008, A1. Location in patent: Page/Page column 69-70
[2] ACS Medicinal Chemistry Letters, 2018,
Tag:5-BROMO INDOLE-7-CARBOXYLIC ACID METHYL ESTER(860624-89-1) Related Product Information
Indole Methyl 1H-indole-7-carboxylate 5-BROMO INDOLE-7-CARBOXYLIC ACID METHYL ESTER