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Home > Encyclopedia > 3-Bromo-5-chloro-1H-indazole

3-Bromo-5-chloro-1H-indazole

3-Bromo-5-chloro-1H-indazole structure

3-Bromo-5-chloro-1H-indazole 

structure
  • CAS No:

    885521-43-7

  • Formula:

    C7H4BrClN2

  • Chemical Name:

    3-Bromo-5-chloro-1H-indazole

  • Synonyms:

    3-Bromo-5-chloro-1H-indazole;3-bromo-5-chloro-2H-indazole;3-Bromo-5-chloro (1H)indazole;3-Bromo-5-chloro(1H)indazole;5-CHLORO-3-BROMO-INDAZOLE;SCHEMBL15332567;CTK5G0751;1H-Indazole,3-bromo-5-chloro-;DTXSID10646256;3-bromanyl-5-chloranyl-2H-indazole

  • Categories:

    Chemical Reagents  >  Organic Reagents

3-Bromo-5-chloro-1H-indazole Basic Attributes

231.48

229.924637

DTXSID10646256

2933990090

Characteristics

28.7

3.2

1.9±0.1 g/cm3

368.5±22.0°C at 760 mmHg

176.6±22.3 °C

1.730

Safety Information

IRRITANT

P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P312, P322, P330, P363, P501

H302

|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P312, P322, P330, P363, and P501|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

3-Bromo-5-chloro-1H-indazole Use and Manufacturing

To a solution of 5-chloro- 1H-indazole (2.5 g, 16.1 mmol) in dichloromethane (150 mL) was added N-bromosuccinimide (2.9 g, 16.6 mmol) and the mixture was stirred at room temperature for 1 hour. The mixture was concentrated under reduced pressure and the residue was dissolved in ethyl acetate (100 mL), washed with water (50 mL) and brine (50 mL), dried over sodium sulfate and concentrated under reduced pressure to afford 3-bromo-5-chloro-1H-indazole (3.7 g, 94percent) as a brown solid. ‘H NMR (DMSO-d6, 400 MHz) 13.63 (s, 1H), 7.67 — 7.59 (m, 2H), 7.49 — 7.44 (m, 1H). TLC: 50percent ethyl acetate/heptane (R1: 0.43).To a solution of 5-chloro- 1H-indazole (2.5 g, 16.1 mmol) in dichloromethane (150 mL) was added N-bromosuccinimide (2.9 g, 16.6 mmol) and the mixture was stirred at room temperature for 1 hour. The mixture was concentrated under reduced pressure and the residue was dissolved in ethyl acetate (100 mL), washed with water (50 mL) and brine (50 mL), dried over sodium sulfate and concentrated under reduced pressure to afford 3-bromo-5-chloro-1H-indazole (3.7 g, 94percent) as a brown solid. ‘H NMR (DMSO-d6, 400 MHz) 13.63 (s, 1H), 7.67 — 7.59 (m, 2H), 7.49 — 7.44 (m, 1H). TLC: 50percent ethyl acetate/heptane (R1: 0.43).

Computed Properties

Molecular Weight:231.48
XLogP3:3.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Exact Mass:229.92464
Monoisotopic Mass:229.92464
Topological Polar Surface Area:28.7
Heavy Atom Count:11
Complexity:155
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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