ChemicalBook > CAS DataBase List > 5'-BROMO-2'-HYDROXY-3'-NITROACETOPHENONE

5'-BROMO-2'-HYDROXY-3'-NITROACETOPHENONE

Product Name
5'-BROMO-2'-HYDROXY-3'-NITROACETOPHENONE
CAS No.
70978-54-0
Chemical Name
5'-BROMO-2'-HYDROXY-3'-NITROACETOPHENONE
Synonyms
5-BROMO-2-HYDROXY-3-NITROACETOPHENONE;3-BROMO-6-HYDROXY-5-NITRO ACETOPHENONE;5'-Bromo-2'-hydroxy-3'-nitroacetophenone;5'-BROMO-2'-HYDROXY-3'-NITROACETOPHENONE;1-(5-BROMO-2-HYDROXY-3-NITROPHENYL)ETHANONE;5'-Bromo-2'-hydroxy-3'-nitroacetophenone >1-(5-Bromo-2-hydroxy-3-nitrophenyl)ethan-1-one;Ethanone, 1-(5-bromo-2-hydroxy-3-nitrophenyl)-;JRH-01018, 1-(5-Bromo-2-hydroxy-3-nitrophenyl)ethanone, 97%
CBNumber
CB9417788
Molecular Formula
C8H6BrNO4
Formula Weight
260.04
MOL File
70978-54-0.mol
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5'-BROMO-2'-HYDROXY-3'-NITROACETOPHENONE Property

Melting point:
129-132 °C(lit.)
Boiling point:
272.9℃
Density 
1.763
Flash point:
118.9℃
storage temp. 
Sealed in dry,Room Temperature
form 
powder to crystal
pka
6.47±0.38(Predicted)
color 
Light yellow to Yellow to Orange
CAS DataBase Reference
70978-54-0(CAS DataBase Reference)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
29145090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

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

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

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

P302+P352IF ON SKIN: wash with plenty of soap and water.

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

Sigma-Aldrich
Product number
534153
Product name
5′-Bromo-2′-hydroxy-3′-nitroacetophenone
Purity
97%
Packaging
25g
Price
$38.7
Updated
2024/03/01
TCI Chemical
Product number
B4556
Product name
5'-Bromo-2'-hydroxy-3'-nitroacetophenone
Purity
>98.0%(GC)(T)
Packaging
5g
Price
$84
Updated
2024/03/01
TCI Chemical
Product number
B4556
Product name
5'-Bromo-2'-hydroxy-3'-nitroacetophenone
Purity
>98.0%(GC)(T)
Packaging
25g
Price
$254
Updated
2024/03/01
Alfa Aesar
Product number
H27331
Product name
5'-Bromo-2'-hydroxy-3'-nitroacetophenone, 97%
Packaging
5g
Price
$36.65
Updated
2024/03/01
Alfa Aesar
Product number
H27331
Product name
5'-Bromo-2'-hydroxy-3'-nitroacetophenone, 97%
Packaging
25g
Price
$107.65
Updated
2024/03/01
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5'-BROMO-2'-HYDROXY-3'-NITROACETOPHENONE Chemical Properties,Usage,Production

Uses

5'-Bromo-2'-hydroxy-3'-nitroacetophenone is used as a chemical reagent in the synthesis of amides and benzoxazoles directly using a sulfate catalyst and microwaves. 1-(5-Bromo-2-hydroxy-3-nitrophen yl)ethanone is used in studies involving HIV-1 integrase inhibitors.

Preparation

Preparation by nitration of 5-bromo-2-hydroxyacetophenone in refluxing carbon tetrachloride (88%).

5'-BROMO-2'-HYDROXY-3'-NITROACETOPHENONE Preparation Products And Raw materials

Raw materials

Preparation Products

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5'-BROMO-2'-HYDROXY-3'-NITROACETOPHENONE Suppliers

TOKYO CHEMICAL INDUSTRY CO., LTD.
Tel
03-36680489
Fax
03-3668-0520
Email
Sales-JP@TCIchemicals.com
Country
Japan
ProdList
28398
Advantage
80

70978-54-0, 5'-BROMO-2'-HYDROXY-3'-NITROACETOPHENONERelated Search:


  • 1-(5-BROMO-2-HYDROXY-3-NITROPHENYL)ETHANONE
  • 3-BROMO-6-HYDROXY-5-NITRO ACETOPHENONE
  • 5'-BROMO-2'-HYDROXY-3'-NITROACETOPHENONE
  • 5-BROMO-2-HYDROXY-3-NITROACETOPHENONE
  • JRH-01018, 1-(5-Bromo-2-hydroxy-3-nitrophenyl)ethanone, 97%
  • 5'-Bromo-2'-hydroxy-3'-nitroacetophenone &gt
  • Ethanone, 1-(5-bromo-2-hydroxy-3-nitrophenyl)-
  • 1-(5-Bromo-2-hydroxy-3-nitrophenyl)ethan-1-one
  • 5'-Bromo-2'-hydroxy-3'-nitroacetophenone
  • 70978-54-0
  • BrC6H2NO2OHCOCH3
  • C8H6BrNO4
  • Building Blocks
  • C7 to C8
  • Carbonyl Compounds
  • Organic Building Blocks
  • Ketones
  • Aromatic Acetophenones & Derivatives (substituted)
  • Building Blocks
  • C7 to C8
  • Carbonyl Compounds
  • Chemical Synthesis
  • Ketones
  • Organic Building Blocks