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6-FLUORO-1H-INDAZOL-3-YLAMINE

Product Name
6-FLUORO-1H-INDAZOL-3-YLAMINE
CAS No.
404827-75-4
Chemical Name
6-FLUORO-1H-INDAZOL-3-YLAMINE
Synonyms
6-Fluoro-2h-indazol-3-amine;6-fluoro-1H-indazol-3-aMine;6-Fluoro-1H-indazol-4-ylamine;6-FLUORO-1H-INDAZOL-3-YLAMINE;1H-Indazol-3-amine, 6-fluoro-;1H-Indazol-3-amine,6-fluoro-(9CI)
CBNumber
CB4296742
Molecular Formula
C7H6FN3
Formula Weight
151.14
MOL File
404827-75-4.mol
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6-FLUORO-1H-INDAZOL-3-YLAMINE Property

storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
Appearance
Light yellow to yellow Solid
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Safety

Hazard Codes 
Xn
Risk Statements 
22
HS Code 
2933998090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
F595163
Product name
6-Fluoro-1h-indazol-3-ylamine
Packaging
250mg
Price
$55
Updated
2021/12/16
TRC
Product number
F595163
Product name
6-Fluoro-1h-indazol-3-ylamine
Packaging
1g
Price
$120
Updated
2021/12/16
Apolloscientific
Product number
PC908712
Product name
6-Fluoro-1H-indazol-3-amine
Purity
97%
Packaging
250mg
Price
$27
Updated
2021/12/16
SynQuest Laboratories
Product number
3H30-3-69
Product name
6-Fluoro-1H-indazol-3-amine
Purity
96%
Packaging
250mg
Price
$29
Updated
2021/12/16
Apolloscientific
Product number
PC908712
Product name
6-Fluoro-1H-indazol-3-amine
Purity
97%
Packaging
1g
Price
$79
Updated
2021/12/16
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6-FLUORO-1H-INDAZOL-3-YLAMINE Chemical Properties,Usage,Production

Synthesis

3939-09-1

404827-75-4

General procedure for the synthesis of 3-amino-6-fluoro-1H-indazole from 2,4-difluorobenzonitrile: 2,4-difluorobenzonitrile (10.00 g, 71.89 mmol) was placed in a 500 mL two-necked round-bottomed flask and n-butanol (200 mL) was added as a solvent. Hydrazine hydrate (70.0 mL, 1443 mmol) was slowly added to the reaction system under nitrogen protection. After addition, the reaction mixture was heated to 150 °C and stirred continuously for 17 hours. After completion of the reaction, the mixture was cooled to room temperature and extracted with ethyl acetate (200 mL x 3). The organic phases were combined, washed sequentially with water (200 mL x 2) and saturated saline (200 mL), dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography with the eluent of petroleum ether/ethyl acetate (v/v=1/2) to afford 3-amino-6-fluoro-1H-indazole as a yellow liquid (4.85 g, 44.7% yield). Mass spectrum (ESI, positive ion mode) m/z: 152.2 ([M+H]+).

References

[1] Patent: WO2018/188590, 2018, A1. Location in patent: Paragraph 00316
[2] Patent: US2009/270405, 2009, A1. Location in patent: Page/Page column 82-83
[3] Patent: WO2011/53292, 2011, A1. Location in patent: Page/Page column 133
[4] Patent: JP5714745, 2015, B2. Location in patent: Paragraph 0264; 0265

6-FLUORO-1H-INDAZOL-3-YLAMINE Preparation Products And Raw materials

Raw materials

Preparation Products

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6-FLUORO-1H-INDAZOL-3-YLAMINE Suppliers

CHEMSTEP
Tel
--
Fax
--
Email
info@chemstep.com
Country
Europe
ProdList
6143
Advantage
51
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View Lastest Price from 6-FLUORO-1H-INDAZOL-3-YLAMINE manufacturers

Career Henan Chemical Co
Product
6-FLUORO-1H-INDAZOL-3-YLAMINE 404827-75-4
Price
US $0.01/KG
Min. Order
1KG
Purity
98%; 99%
Supply Ability
500g;1kg; 25kg
Release date
2020-01-09

404827-75-4, 6-FLUORO-1H-INDAZOL-3-YLAMINERelated Search:


  • 6-FLUORO-1H-INDAZOL-3-YLAMINE
  • 6-fluoro-1H-indazol-3-aMine
  • 1H-Indazol-3-amine,6-fluoro-(9CI)
  • 1H-Indazol-3-amine, 6-fluoro-
  • 6-Fluoro-2h-indazol-3-amine
  • 6-Fluoro-1H-indazol-4-ylamine
  • 404827-75-4
  • HALIDE