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METHYL 1-ACETYL-1H-INDAZOLE-5-CARBOXYLATE

Product Name
METHYL 1-ACETYL-1H-INDAZOLE-5-CARBOXYLATE
CAS No.
239075-26-4
Chemical Name
METHYL 1-ACETYL-1H-INDAZOLE-5-CARBOXYLATE
Synonyms
methyl 1-acetylindazole-5-carboxylate;METHYL 1-ACETYL-1H-INDAZOLE-5-CARBOXYLATE;1H-Indazole-5-carboxylic acid, 1-acetyl-, methyl ester
CBNumber
CB41502572
Molecular Formula
C11H10N2O3
Formula Weight
218.21
MOL File
239075-26-4.mol
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METHYL 1-ACETYL-1H-INDAZOLE-5-CARBOXYLATE Property

storage temp. 
2-8°C
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
M220260
Product name
Methyl1-Acetyl-1H-indazole-5-carboxylate
Packaging
100mg
Price
$75
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0384670
Product name
METHYL-1-ACETYL-1H-INDAZOLE-5-CARBOXYLATE
Purity
95.00%
Packaging
5MG
Price
$500.21
Updated
2021/12/16
AK Scientific
Product number
1679AB
Product name
Methyl1-acetyl-1H-indazole-5-carboxylate
Packaging
5g
Price
$278
Updated
2021/12/16
Chemenu
Product number
CM150142
Product name
Methyl1-acetyl-1H-indazole-5-carboxylate
Purity
95%
Packaging
10g
Price
$292
Updated
2021/12/16
Ambeed
Product number
A532663
Product name
Methyl1-acetyl-1H-indazole-5-carboxylate
Purity
95+%
Packaging
25g
Price
$567
Updated
2021/12/16
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METHYL 1-ACETYL-1H-INDAZOLE-5-CARBOXYLATE Chemical Properties,Usage,Production

Synthesis

18595-14-7

108-24-7

239075-26-4

Methyl 4-amino-3-methylbenzoate (2.0 g, 12.03 mmol) was dissolved in chloroform (25 mL), and ethanoic anhydride (2.12 g, 30.07 mmol) was added slowly and dropwise at 0 °C. The reaction mixture was stirred at room temperature for 1 h. Potassium acetate (250 mg, 3.61 mmol) and isoamyl nitrite (2.23 mL, 24.06 mmol) were added sequentially. The reaction system was warmed up to 70 °C and stirred at reflux for 18 hours. Upon completion of the reaction, it was diluted by adding excess dichloromethane. The mixture was washed sequentially with saturated aqueous sodium bicarbonate, dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by column chromatography to afford the intermediate methyl 1-acetyl-1H-indazole-5-carboxylate (1.2 g, 5.50 mmol).

References

[1] Chemical Communications, 2012, vol. 48, # 94, p. 11558 - 11560
[2] Patent: WO2014/129796, 2014, A1. Location in patent: Paragraph 1225-1227

METHYL 1-ACETYL-1H-INDAZOLE-5-CARBOXYLATE Preparation Products And Raw materials

Raw materials

Preparation Products

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METHYL 1-ACETYL-1H-INDAZOLE-5-CARBOXYLATE Suppliers

Alchem Pharmtech,Inc.
Tel
8485655694
Email
sales@alchempharmtech.com
Country
United States
ProdList
63687
Advantage
58
Synthonix Inc
Tel
--
Fax
--
Email
info@synthonix.com
Country
United States
ProdList
6872
Advantage
58
Combi-Blocks Inc.
Tel
--
Fax
--
Email
sales@combi-blocks.com
Country
United States
ProdList
6618
Advantage
69
AlliChem, LLC
Tel
--
Fax
--
Email
sales@allichemllc.com
Country
United States
ProdList
6516
Advantage
60

239075-26-4, METHYL 1-ACETYL-1H-INDAZOLE-5-CARBOXYLATERelated Search:


  • METHYL 1-ACETYL-1H-INDAZOLE-5-CARBOXYLATE
  • methyl 1-acetylindazole-5-carboxylate
  • 1H-Indazole-5-carboxylic acid, 1-acetyl-, methyl ester
  • 239075-26-4