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Home > Encyclopedia > 3-bromo-1H-pyrrolo[3,2-b]pyridine

3-bromo-1H-pyrrolo[3,2-b]pyridine

3-bromo-1H-pyrrolo[3,2-b]pyridine structure

3-bromo-1H-pyrrolo[3,2-b]pyridine 

structure
  • CAS No:

    23688-47-3

  • Formula:

    C7H5BrN2

  • Chemical Name:

    3-bromo-1H-pyrrolo[3,2-b]pyridine

  • Synonyms:

    3-Bromo-1H-pyrrolo[3,2-b]pyridine;3-BROMO-4-AZAINDOLE;1H-Pyrrolo[3,2-b]pyridine, 3-bromo-;SCHEMBL569155;CTK4F2041;DTXSID50657104;KS-00000ID5;ANW-49878;MFCD10697525;ZINC30677857

  • Categories:

    Chemical Reagents  >  Organic Reagents

3-bromo-1H-pyrrolo[3,2-b]pyridine Basic Attributes

197.04

195.963608

DTXSID50657104

Characteristics

28.7

1.8

1.8±0.1 g/cm3

232-238 °C

346.3ºC at 760 mmHg

163.2±22.3 °C

1.728

0.000117mmHg at 25°C

Safety Information

P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, 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, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 3 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

3-bromo-1H-pyrrolo[3,2-b]pyridine Use and Manufacturing

(R)-3-Pyrrolidin-2-ylmethyl-1H-pyrrolo[3, 2-b]pyridine.(Compound 88) Example 3 3-Bromo-4-Azaindole[00147] solution of 0.9707g (8.21 mmol) of 4-azaindole in 50 ml. of acetonitrile was placed in a 250 ml. three-neck round-bottom flask equipped with a magnetic stirrer, thermocouple, nitrogen bleed, and cooling ice bath. A total of 5.5187g (24.7 mmol, 3 eq.) of solid CuBrTo a stirredsolution of 1H-pyrrolo[3, 2-b]pyridine(1.0 g, 8.47 mmol) in dry DMF (10 ml) was added N-bromosuccinimide(1.51 g, 8.48 mmol) at 0 °C and the resultant mixture was stirredfor 1 h at the same temperature. The reaction mixture was dilutedwith saturated sodium bicarbonate solution (50 ml) and extracted withethyl acetate (2 x 150 ml). The combined organic layers were washedwith brine (50 ml) and dried (Na(R)-3-Pyrrolidin-2-ylmethyl-1H-pyrrolo[3, 2-b]pyridine.(Compound 88) Example 3 3-Bromo-4-Azaindole[00147] solution of 0.9707g (8.21 mmol) of 4-azaindole in 50 ml. of acetonitrile was placed in a 250 ml. three-neck round-bottom flask equipped with a magnetic stirrer, thermocouple, nitrogen bleed, and cooling ice bath. A total of 5.5187g (24.7 mmol, 3 eq.) of solid CuBrTo a stirredsolution of 1H-pyrrolo[3, 2-b]pyridine(1.0 g, 8.47 mmol) in dry DMF (10 ml) was added N-bromosuccinimide(1.51 g, 8.48 mmol) at 0 °C and the resultant mixture was stirredfor 1 h at the same temperature. The reaction mixture was dilutedwith saturated sodium bicarbonate solution (50 ml) and extracted withethyl acetate (2 x 150 ml). The combined organic layers were washedwith brine (50 ml) and dried (Na

Computed Properties

Molecular Weight:197.03
XLogP3:1.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Exact Mass:195.96361
Monoisotopic Mass:195.96361
Topological Polar Surface Area:28.7
Heavy Atom Count:10
Complexity:129
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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