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Home > Encyclopedia > 2-Amino-5-bromophenol

2-Amino-5-bromophenol

2-Amino-5-bromophenol structure

2-Amino-5-bromophenol 

structure
  • CAS No:

    38191-34-3

  • Formula:

    C6H6BrNO

  • Chemical Name:

    2-Amino-5-bromophenol

  • Synonyms:

    Phenol,2-amino-5-bromo-;2-Amino-5-bromophenol;4-Bromo-2-hydroxyaniline;5-Bromo-2-aminophenol

  • Categories:

    Pharmaceutical Intermediates  >  Heterocyclic Compound

Description

white to light yellow solid

2-Amino-5-bromophenol Basic Attributes

188.02

188.02

DTXSID80558877

2922299090

Characteristics

46.2

1.6

white to light yellow solid

1.8±0.1 g/cm3

146-147 °C

265°C at 760 mmHg

114.1±23.2 °C

1.677

Safety Information

43

36/37

P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501

H315

|Warning|H302 (50%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 2 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

2-Amino-5-bromophenol Use and Manufacturing

3-Bromo-6-nitrophenol (0.292 gms, 1. 34 mmole) was stirred in an 0.5percent aqueous sodium hydroxide solution (30 mL). Sodium hydrosulphite (2.00 gms of 85percent, 9.76 mmole) was added to the reaction flask and this was stirred at room temperature for 15 minutes. The reaction flask was then acidified with diluted hydrochloric acid until a pH of 5 was obtained. The reaction was then extracted three times with 40 mL portions of diethyl ether, the combined organic layers dried over anhydrous sodium sulfate, and concentrated to provide crude 2-amino-5-bromophenol (0.533 gms, m. p. 99.5-100. 5 C), which was recrystallized from ethyl ether/hexanes to provide the pure product (0.151 gms, 0.80 mmole, 60percent yield; m. p. 125-127 C (decompose) (reported m. p. 149.5-150. 5 C (Boyland, E et al., 1954) ;'H NMR (CD3CN, 500 MHz) 8 7.08 (bs, 1H), 6.82 (d, 1H, J= 2 Hz), 6.78 (dd, 1H, J= 8, 2 Hz), 6.56 (d, 1H, J= 8 Hz), 4.03 (bs, 2H); IR (KBr) 3496 (broad), 3377, 3298, 1598, 1502, 1431, 1269, 1210, 916, 877 cm'') 5aposINTERMEDIATE B3 2-Amino-5-bromophenol A suspension of iV-(4-bromo-2-hydroxyphenyl)acetamide (Intermediate B2; 1.35 g, 5.87 mmol) in EtOH (30 mL) and 3 M HCl (30 mL) was heated to 100

Computed Properties

Molecular Weight:188.02
XLogP3:1.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Exact Mass:186.96328
Monoisotopic Mass:186.96328
Topological Polar Surface Area:46.2
Heavy Atom Count:9
Complexity:99.1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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