ChemicalBook > CAS DataBase List > 4-broMo-5-Methoxy-1H-indazole

4-broMo-5-Methoxy-1H-indazole

Product Name
4-broMo-5-Methoxy-1H-indazole
CAS No.
1192004-62-8
Chemical Name
4-broMo-5-Methoxy-1H-indazole
Synonyms
4-Bromo-5-methoxyindazole;4-broMo-5-Methoxy-1H-indazole;1H-Indazole, 4-bromo-5-methoxy-
CBNumber
CB72597848
Molecular Formula
C8H7BrN2O
Formula Weight
227.06
MOL File
1192004-62-8.mol
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4-broMo-5-Methoxy-1H-indazole Property

Boiling point:
363.4±22.0 °C(Predicted)
Density 
1.678±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
12.39±0.40(Predicted)
Appearance
Light yellow to yellow Solid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

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
B679498
Product name
4-Bromo-5-methoxy-1H-indazole
Packaging
10mg
Price
$45
Updated
2021/12/16
TRC
Product number
B679498
Product name
4-Bromo-5-methoxy-1H-indazole
Packaging
50mg
Price
$90
Updated
2021/12/16
TRC
Product number
B679498
Product name
4-Bromo-5-methoxy-1H-indazole
Packaging
100mg
Price
$130
Updated
2021/12/16
Crysdot
Product number
CD11335021
Product name
4-Bromo-5-methoxy-1H-indazole
Purity
95+%
Packaging
250mg
Price
$90
Updated
2021/12/16
Crysdot
Product number
CD11335021
Product name
4-Bromo-5-methoxy-1H-indazole
Purity
95+%
Packaging
1g
Price
$226
Updated
2021/12/16
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4-broMo-5-Methoxy-1H-indazole Chemical Properties,Usage,Production

Synthesis

29237-10-3

1192004-62-8

General procedure for the synthesis of 4-bromo-5-methoxy-1H-indazole from 3-bromo-4-methoxy-2-methylaniline: 1. 3-Bromo-4-methoxy-2-methylaniline (19.06 g) was dissolved in acetonitrile (250 mL), acetic anhydride (18.9 mL) was added slowly, and the reaction mixture was stirred for 1 hour at room temperature. 2. Potassium acetate (2.60 g) and amyl nitrite (22.3 g) were added to the reaction mixture and heated to reflux for 8 hours. 3. After completion of the reaction, the reaction mixture was concentrated and 6 M hydrochloric acid (200 mL) was added to the residue and heated to reflux overnight. 4. The reaction mixture was neutralized with 8 M sodium hydroxide and subsequently extracted with ethyl acetate. 5. The ethyl acetate layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. 6. The residue was dissolved in tetrahydrofuran, treated with activated charcoal, filtered to remove the activated charcoal and the filtrate was concentrated. 7. The residue was crystallized with diisopropyl ether, the crystals were collected by filtration, washed with diisopropyl ether and dried to obtain the target compound 4-bromo-5-methoxy-1H-indazole (10.42 g, yield 52%) as yellow crystals. Melting point: 178-180°C. Mass spectrum (MS): 229 (MH+).

References

[1] Patent: EP2266983, 2010, A1. Location in patent: Page/Page column 48
[2] Patent: US2009/286800, 2009, A1. Location in patent: Page/Page column 109; 111

4-broMo-5-Methoxy-1H-indazole Preparation Products And Raw materials

Raw materials

Preparation Products

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4-broMo-5-Methoxy-1H-indazole Suppliers

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1192004-62-8, 4-broMo-5-Methoxy-1H-indazoleRelated Search:


  • 4-broMo-5-Methoxy-1H-indazole
  • 1H-Indazole, 4-bromo-5-methoxy-
  • 4-Bromo-5-methoxyindazole
  • 1192004-62-8