5-FLUORO-1H-INDAZOLE

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Products Intro: CAS:348-26-5
Purity:97% Package:g-Kg
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CAS:348-26-5
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Products Intro: Product Name:5-Fluoro-1H-indazole
CAS:348-26-5
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Company Name: CONIER CHEM AND PHARMA LIMITED
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Products Intro: Product Name:5-fluoro-1h-indazole
CAS:348-26-5
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5-FLUORO-1H-INDAZOLE manufacturers

  • 5-FLUORO-1H-INDAZOLE
  • 5-FLUORO-1H-INDAZOLE pictures
  • $0.00 / 1KG
  • 2019-07-06
  • CAS:348-26-5
  • Min. Order: 1KG
  • Purity: 98%
  • Supply Ability: 150KG
5-FLUORO-1H-INDAZOLE Basic information
Product Name:5-FLUORO-1H-INDAZOLE
Synonyms:5-FLUORO-1H-INDAZOLE;1H-Indazole, 5-fluoro-;5-fluoro-1H-indazole(SALTDATA: FREE);5-Fluoroindazole;5-Fluoro-1H-indazole
CAS:348-26-5
MF:C7H5FN2
MW:136.13
EINECS:
Product Categories:Building Blocks;Chemical Synthesis;Fluorinated Building Blocks;Halogenated Heterocycles;Heterocyclic Building Blocks;Heterocyclic Fluorinated Building Blocks;Other Fluorinated Heterocycles;Others;Indoles and derivatives;Halogenated Heterocycles;Heterocyclic Building Blocks;Indazoles
Mol File:348-26-5.mol
5-FLUORO-1H-INDAZOLE Structure
5-FLUORO-1H-INDAZOLE Chemical Properties
Melting point 119-125 °C
Boiling point 274.9±13.0 °C(Predicted)
density 1.370±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka12.90±0.40(Predicted)
form solid
color Beige
CAS DataBase Reference348-26-5(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-22
Safety Statements 26-36/37/39
WGK Germany 3
HazardClass IRRITANT
HS Code 2933998090
MSDS Information
5-FLUORO-1H-INDAZOLE Usage And Synthesis
Uses5-Fluoro-1H-indazole(Indazole compound) or its physiologically acceptable derivative are respectively provided with the effect for inhibiting Rho kinase activity;It is thin with promoting The effect of born of the same parents' glucose consumption.
Synthesis
1-(5-fluoro-1H-indazol-1-yl)ethanone

141071-11-6

5-FLUORO-1H-INDAZOLE

348-26-5

Step 2: Preparation of 5-fluoro-1H-indazole 1-(5-Fluoro-1H-indazol-1-yl)ethan-1-one (2.1 g, 11.8 mmol) was dissolved in a mixture of methanol (20 mL) and concentrated hydrochloric acid (10 mL), heated to 50 °C and maintained for 2 hours. Upon completion of the reaction, the reaction mixture was evaporated to dryness under reduced pressure. The residue was alkalized with saturated sodium bicarbonate solution and extracted with ethyl acetate, the organic phase was washed with water and concentrated to afford the target product 5-fluoro-1H-indazole (1.6 g, 100% yield). The purity was analyzed by LCMS and was 95.9%; m/z = 137.2.

References[1] Patent: WO2015/193846, A1. Location in patent: Page/Page column 80
[1] Patent: , 2015, . Location in patent: Page/Page column 80
5-FLUORO-1H-INDAZOLE Preparation Products And Raw materials
Raw materials1-(5-fluoro-1H-indazol-1-yl)ethanone-->Methanol-->Hydrochloric acid
Tag:5-FLUORO-1H-INDAZOLE(348-26-5) Related Product Information
5-fluoro-1H-indazol-3-amine METHYL 5-FLUORO-1H-INDAZOLE-3-CARBOXYLATE 5-FLUORO-1H-INDAZOLE 5-Fluoro-3-iodo-1H-indazole 5-FLUORO-1-METHYL-1H-INDAZOLE-3-CARBOXYLIC ACID 5-FLUORO-1H-INDAZOLE-3-CARBOXYLIC ACID 4-BROMO-6-FLUORO (1H)INDAZOLE 4-FLUORO (1H)INDAZOLE 7-FLUORO INDAZOLE 1H-Indazol-5-amine,6-fluoro-(9CI) 3-Amino-4-fluoro-1-methylindazole 6-FLUORO (1H)INDAZOLE Indazole 1-BOC-3-BROMO-5-FLUORO-INDAZOLE (5-FLUORO-1H-INDAZOL-3-YL)-METHANOL 5,6-DIFLUORO-1H-INDAZOLE-3-CARBONITRILE (5-FLUORO-1H-INDAZOL-3-YL)-ACETIC ACID ETHYL ESTER ETHYL 5,6-DIFLUORO-1H-INDAZOLE-3-CARBOXYLATE

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