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43120-28-1

  • Product Name:1H-INDAZOLE-3-CARBOXYLIC ACID METHYL ESTER
  • Molecular Formula:C9H8N2O2
  • Molecular Weight:176.175
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Product Details

pd_meltingpoint:162-163℃

Purity:99%

Chinese Manufacturer Supply 1H-INDAZOLE-3-CARBOXYLIC ACID METHYL ESTER 43120-28-1 On Stock with Competitive Price

  • Molecular Formula:C9H8N2O2
  • Molecular Weight:176.175
  • Vapor Pressure:6.24E-05mmHg at 25°C 
  • Melting Point:162-163℃ 
  • Refractive Index:1.648 
  • Boiling Point:345.2 °C at 760 mmHg 
  • PKA:11.93±0.40(Predicted) 
  • Flash Point:162.6 °C 
  • PSA:54.98000 
  • Density:1.325 g/cm3 
  • LogP:1.34950 

1H-INDAZOLE-3-CARBOXYLIC ACID METHYL ESTER(Cas 43120-28-1) Usage

InChI:InChI=1/C9H8N2O2/c1-13-9(12)8-6-4-2-3-5-7(6)10-11-8/h2-5H,1H3,(H,10,11)

43120-28-1 Relevant articles

Regioselective N-alkylation of the 1H-indazole scaffold; ring substituent and N-alkylating reagent effects on regioisomeric distribution

Alam, Ryan M.,Keating, John J.

supporting information, p. 1939 - 1951 (2021/08/23)

The indazole scaffold represents a promi...

Preparation methods of 1H-indazol-3-carboxylic acid derivative, granisetron and lonidamine

-

Paragraph 0072-0077; 0097-0102; 0122; 0133-0135, (2021/05/12)

The invention relates to preparation met...

NovelN-transfer reagent for converting α-amino acid derivatives to α-diazo compounds

Lu, Guan-Han,Huang, Tzu-Chia,Hsueh, Hsiao-Chin,Yang, Shin-Cherng,Cho, Ting-Wei,Chou, Ho-Hsuan

, p. 4839 - 4842 (2021/05/25)

A novel universalN-transfer reagent for ...

NOVEL ARYLALKYL PYRAZOLE COMPOUNDS AS INDOLEAMINE 2,3-DIOXYGENASE INHIBITORS

-

Page/Page column 97-98, (2020/05/21)

Disclosed herein are compounds of formul...

43120-28-1 Process route

methanol
67-56-1

methanol

1H-Indazole-3-carboxylic acid
4498-67-3

1H-Indazole-3-carboxylic acid

methyl 1H-indazole-3-carboxylate
43120-28-1

methyl 1H-indazole-3-carboxylate

Conditions
Conditions Yield
With sulfuric acid; for 2h; Heating;
98%
With sulfuric acid; for 2h; Reflux;
95%
With thionyl chloride; for 3h; Reflux;
95%
With thionyl chloride; at 0 ℃; for 1.5h; Reflux;
94%
With thionyl chloride; at 0 - 20 ℃;
93%
With thionyl chloride; at 20 ℃; Cooling with ice;
93%
With thionyl chloride; at 0 ℃; for 5h; Reflux;
92%
With sulfuric acid; for 16h; Reflux;
92%
methanol; 1H-Indazole-3-carboxylic acid; With sulfuric acid; at 80 ℃; for 16h;
With sodium hydrogencarbonate; In water; ethyl acetate;
90.1%
With sulfuric acid; for 24h; Reflux;
88%
methanol; With acetyl chloride; for 0.166667h; Cooling with ice;
1H-Indazole-3-carboxylic acid; at 20 ℃;
85%
With sulfuric acid; at 80 ℃;
82%
methanol; 1H-Indazole-3-carboxylic acid; With sulfuric acid; for 4h; Reflux;
With sodium hydrogencarbonate; In water; ethyl acetate;
78%
With sulfuric acid; for 10h; Heating / reflux;
48%
With sulfuric acid;
With hydrogenchloride; Heating;
sulfuric acid; Heating / reflux;
With sulfuric acid; at 80 ℃; for 24h;
With sulfuric acid;
With thionyl chloride; at 20 ℃; for 24h;
With sulfuric acid; for 20h; Heating / reflux;
With sulfuric acid; In water; at 80 ℃; for 24h;
With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 24h;
With sulfuric acid; Reflux;
With sulfuric acid; for 5h; Reflux;
With sulfuric acid; at 60 ℃;
22.76 g
With sulfuric acid; for 4h; Reflux;
With thionyl chloride; at 0 - 80 ℃; for 2h;
methanol; With acetyl chloride; for 0.5h; Cooling with ice;
1H-Indazole-3-carboxylic acid; for 4h; Reflux;
2-aminophenylacetic acid methyl ester
35613-44-6

2-aminophenylacetic acid methyl ester

methyl 1H-indazole-3-carboxylate
43120-28-1

methyl 1H-indazole-3-carboxylate

Conditions
Conditions Yield
With tert.-butylnitrite; acetic acid; In acetonitrile; at 20 - 25 ℃; for 0.5h; Flow reactor;
92%
Multi-step reaction with 2 steps
1: sodium nitrite / water; tetrahydrofuran / 0.25 h / -5 °C
2: potassium carbonate / water; tetrahydrofuran / 0.25 h / 0 - 20 °C
With potassium carbonate; sodium nitrite; In tetrahydrofuran; water;

43120-28-1 Upstream products

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43120-28-1 Downstream products

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    1(2)H-indazole-3-carboxylic acid dimethylamide

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    2-Methylindazole-3-carboxylic acid

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    3-methoxycarbonyl-2-methylisoindazole

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    3-(hydroxymethyl)-1H-indazole

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