ChemicalBook Product Catalog Chemical Reagents Organic reagents Phenols 5-METHOXY-2-NITROPHENOL

5-METHOXY-2-NITROPHENOL

5-METHOXY-2-NITROPHENOL Basic information
Product Name:5-METHOXY-2-NITROPHENOL
Synonyms:TIMTEC-BB SBB008609;5-METHOXY-2-NITROPHENOL 98%;5-METHOZY-2-NITROPHENOL;5-METHOXY-2-NITROPHENOL;3-HYDROXY-4-NITROANISOLE;phenol, 5-methoxy-2-nitro-;2-Hydroxy-4-methoxynitrobenzene, 3-Hydroxy-4-nitrotoluene;5-Methoxy-2-nitrophenol, 98% 1GR
CAS:704-14-3
MF:C7H7NO4
MW:169.13
EINECS:
Product Categories:Aromatic Phenols;Organic Building Blocks;Oxygen Compounds;Phenols;Building Blocks;C6 to C8;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds
Mol File:704-14-3.mol
5-METHOXY-2-NITROPHENOL Structure
5-METHOXY-2-NITROPHENOL Chemical Properties
Melting point 92-94 °C(lit.)
Boiling point 298.4°C (rough estimate)
density 1.367
refractive index 1.5830 (rough estimate)
storage temp. Sealed in dry,Room Temperature
solubility Chloroform (Slightly), Methanol (Slightly)
pka6.95±0.13(Predicted)
form Powder or Crystals
color Yellow
CAS DataBase Reference704-14-3(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 37/38-41-36/37/38
Safety Statements 26-36-37/39
WGK Germany 3
HazardClass IRRITANT
HS Code 29095000
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
5-METHOXY-2-NITROPHENOL Usage And Synthesis
Chemical Propertiesyellow crystals or powder
Uses5-Methoxy-2-nitrophenol is a reagent in the synthesis of conformationally constrained spirocycles, which are used as CCR1 antagonists. 5-Methoxy-2-nitrophenol is also used in the preparation of phenylsulfonyl aminophenoxybenzoates which can serve as EP1 receptor antagonists.
Synthesis Reference(s)Synthetic Communications, 23, p. 343, 1993 DOI: 10.1080/00397919308009786
5-METHOXY-2-NITROPHENOL Preparation Products And Raw materials
Preparation Products3-Methoxy-2-nitrophenol-->3-methoxy-4-nitrophenol
EOSIN B 2-((1R)-1-AMINO-2-METHYLPROPYL)-6-METHOXY-4-NITROPHENOL 3-BROMO-2,6-DIMETHOXY-5-NITROBENZOIC ACID 3,4,5-TRIMETHOXY-2-NITROBENZOIC ACID METHYL 2,6-DIMETHOXY-3-NITROBENZOATE 2-BROMO-4-METHOXY-6-NITROPHENOL 1,3,5-TRIMETHOXY-2-NITROBENZENE 1,3,5-TRIMETHOXY-2,4-DINITROBENZENE 3-BROMO-2,6-DIMETHOXY-5-NITROBENZAMIDE 1-(2-HYDROXY-6-METHOXY-3-NITROPHENYL)ETHAN-1-ONE 2-((1S)-1-AMINO-2,2,2-TRIFLUOROETHYL)-6-METHOXY-4-NITROPHENOL 5-METHOXY-6,7,8-TRINITRO-2,3-DIHYDRO-1,4-BENZODIOXINE 2-((1R)-1-AMINOBUTYL)-6-METHOXY-4-NITROPHENOL 2,6-DIMETHOXY-3-NITROBENZAMIDE 3-NITRO-2,6-DI(4-NITROPHENOXY)BENZONITRILE 2-((1S)-1-AMINOBUTYL)-6-METHOXY-4-NITROPHENOL 2-((1S)AMINOCYCLOPROPYLMETHYL)-6-METHOXY-4-NITROPHENOL 3-CHLORO-2,6-DIMETHOXY-5-NITROBENZAMIDE
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