4-Nitrophthalic anhydride

4-Nitrophthalic anhydride Basic information
Product Name:4-Nitrophthalic anhydride
Synonyms:5-NITRO-ISOBENZOFURAN-1,3-DIONE;TIMTEC-BB SBB008431;1,3-Isobenzofurandione, 5-nitro-;4-Nitrophthalic acid anhydride;4-nitrophthalicacidanhydride;4-NITROPHTHALIC ANHYDRIDE;4-Nitro Phthalic Anhydride p-Nitro Phthalic Anhydride;4-Nitrophthalicanhydride,95%
CAS:5466-84-2
MF:C8H3NO5
MW:193.11
EINECS:226-776-2
Product Categories:Aromatics;Heterocycles;Carboxylic Acid Anhydrides;Organic Building Blocks;Intermediates & Fine Chemicals;Pharmaceuticals;Anhydride Monomers;Monomers;Polymer Science;Carbonyl Compounds
Mol File:5466-84-2.mol
4-Nitrophthalic anhydride Structure
4-Nitrophthalic anhydride Chemical Properties
Melting point 116-120 °C(lit.)
Boiling point 197 °C / 8mmHg
density 1.6392 (rough estimate)
refractive index 1.4700 (estimate)
storage temp. Inert atmosphere,Room Temperature
solubility Acetone (Slightly), Chloroform (Slightly), Methanol (Slightly)
form Solid
color Pale Beige
Water Solubility Hydrolysis
Sensitive Moisture Sensitive
BRN 179682
CAS DataBase Reference5466-84-2(CAS DataBase Reference)
NIST Chemistry Reference4-Nitrophthalic anhydride(5466-84-2)
EPA Substance Registry System5-Nitrophthalic anhydride (5466-84-2)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-20/22
Safety Statements 26-36-36/37/39-22
WGK Germany 3
RTECS TI3328000
10-21
TSCA Yes
HS Code 29173990
MSDS Information
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4-Nitrophthalic anhydride Usage And Synthesis
Chemical Propertiesoff-white to light yellow-brown powder. Soluble in hot alcohol, hot acetic acid and acetone, insoluble in water.
Uses5-Nitrophthalic Anhydride is used in the preparation of phthalic acids as well as compounds with anticonvulsant activities.
Uses4-Nitrophthalic anhydride is used an an intermediate for the synthesis of a benzimidazole PARP inhibitor I (succinate salt) (ABT-472).
Preparation4-Nitrophthalic anhydride is synthesized by hydrolysis of 4-nitrophthalimide and then dehydration. The 4-nitrophthalimide was added to the sodium hydroxide solution, heated and boiled for 15min. Adjust pH to 6-8 with nitric acid, and add nitric acid to boil for 5 min. Cooling, filtering, the filtrate was extracted with ether, the extract was dried and then the ether was evaporated, that is, 4-Nitrophthalic anhydride crystals were precipitated. Yield 95%.
General DescriptionYellow powder.
Air & Water ReactionsReacts with water. The organic acids produced by this reaction are significantly more soluble in water.
Reactivity Profile4-Nitrophthalic anhydride reacts exothermically with water. The reactions are usually slow, but might become violent if local heating accelerates their rate. Acids accelerate the reaction with water. Incompatible with acids, strong oxidizing agents, alcohols, amines, and bases.
Fire HazardFlash point data for 4-Nitrophthalic anhydride are not available, however 4-Nitrophthalic anhydride is probably combustible.
Purification MethodsDistil the anhydride in a vacuum and/or recrystallise it from *C6H6 or Et2O/pet ether. Dry it in vacuo. It forms addition compounds with anthracene (m 118o), and phenanthrene (m 96o). [Beilstein 17 III/IV 6150, 17/11 V 267.]
PrecautionsMoisture Sensitive. Store away from strong bases and oxidizing agents. Incompatible with water, bases, strong acids and oxidizing agents.
PHTHALAMIDE O-Phthalimide Phthalonitrile 3-Fluorophthalic anhydride Maleic anhydride 3-Nitroacetophenone cis-1,2,3,6-Tetrahydrophthalic anhydride TRITON Dibutyl phthalate Phthalic anhydride 4-Nitrophenol Nitrobenzene 3-NITROPHTHALIC ANHYDRIDE ,99+%,3-NITROPHTHALIC ANHYDRIDE 2-Nitrobenzaldehyde Isatoic Anhydride Dimethyl phthalate 2-Nitrobenzoic acid Nitroethane

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