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2,3-Naphthalenedicarboxylic Anhydride

2,3-Naphthalenedicarboxylic Anhydride Structure
CAS No.
716-39-2
Chemical Name:
2,3-Naphthalenedicarboxylic Anhydride
Synonyms
EA253;2,3-NAPHTHALI;2,3-NAPHTHALIC ANHYDRIDE;naphtho[2,3-c]furan-1,3-dione;benzo[f][2]benzofuran-1,3-dione;benzo[f]isobenzofuran-1,3-quinone;2,3-Napthalenedicarboxycanhydride;2,3-NAPHTHALENEDICARBOXYLIC ANHYDRIDE;2,3-NaphthalenedicarboxylicAnhydride>1,3-Dihydronaphtho[2,3-c]furan-1,3-dione
CBNumber:
CB9286597
Molecular Formula:
C12H6O3
Molecular Weight:
198.17
MOL File:
716-39-2.mol
Modify Date:
2023/8/31 10:02:46

2,3-Naphthalenedicarboxylic Anhydride Properties

Melting point 246 °C
Boiling point 275-280 °C(Press: 100 Torr)
Density 1.449±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility Chloroform (Slightly), Ethyl Acetate (Slightly)
form Solid
color Pale Beige
Stability Moisture Sensitive
InChI InChI=1S/C12H6O3/c13-11-9-5-7-3-1-2-4-8(7)6-10(9)12(14)15-11/h1-6H
InChIKey IZJDCINIYIMFGX-UHFFFAOYSA-N
SMILES O1C(=O)C2=CC3C(C=C2C1=O)=CC=CC=3
EPA Substance Registry System Naphtho[2,3-c]furan-1,3-dione (716-39-2)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H332-H335
Precautionary statements  P261-P280-P305+P351+P338
Safety Statements  22-24/25
HS Code  2917.39.7000

2,3-Naphthalenedicarboxylic Anhydride price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemicals (India) N0530 2,3-Naphthalenedicarboxylic Anhydride min. 95.0 % 716-39-2 25G ₹8600 2022-05-26 Buy
TCI Chemicals (India) N0530 2,3-Naphthalenedicarboxylic Anhydride min. 95.0 % 716-39-2 250G ₹13200 2022-05-26 Buy
Product number Packaging Price Buy
N0530 25G ₹8600 Buy
N0530 250G ₹13200 Buy

2,3-Naphthalenedicarboxylic Anhydride Chemical Properties,Uses,Production

Description

A few years ago, the product was still synthesized from the corresponding diacid, but in recent years, it has been difficult to find the shadow of the diacid in the market, and the sales of this product have been repeatedly restricted, resulting in high prices.

Uses

2,3-Naphthalic anhydride is used as a reagent to synthesize analogues of Thalidomide (T338850), an inhibitor of tumour necrosis factor that was once abandoned because it caused birth defects, but is currently used as an inhibitor of angiogenesis in patients with multiple myeloma.

Preparation

Add anhydrous tetrahydrofuran (its mass ratio to maleic anhydride is 1.5:1), cat-1 (0.05 mole), maleic anhydride (1 mole), and o-phthalaldehyde (1.5 mole) to the reactor. After adding triethylamine (5 moles), adjust the temperature below -40°C. Silicon tetrachloride (4 moles) was added dropwise to the reaction system and the reaction was placed at -40 °C for 4 h. The mixture was heated to reflux for 20 h. After the end of the reaction, concentrating the solution to a certain concentration with diatomaceous earth filtration. A light yellow solid, namely 2,3-Naphthalenedicarboxylic Anhydride, is obtained by precipitation, filtration, recrystallization and drying. Its yield reaches 88%.
2,3-Naphthalenedicarboxylic Anhydride

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2,3-NAPHTHALENEDICARBOXYLIC ANHYDRIDE 1,3-Dihydronaphtho[2,3-c]furan-1,3-dione benzo[f][2]benzofuran-1,3-dione benzo[f]isobenzofuran-1,3-quinone 2,3,NAPHTHALENEDICARBOXYLIC ACIDANHYDRIDE naphtho[2,3-c]furan-1,3-dione 2,3-NAPHTHALIC ANHYDRIDE 2,3-NAPHTHALI 2,3-NaphthalenedicarboxylicAnhydride> 2,3-NAPHTHALENEDICARBOXYLIC ANHYDRIDE ISO 9001:2015 REACH EA253 2,3-Napthalenedicarboxycanhydride 716-39-2 Exciton Chirality CD Method (for Primary Amino Groups) Enantiomer Excess & Absolute Conefiguration Determination Absolute Conefiguration Determination (Exciton Chirality CD Method) Absolute Configuration Determination (Exciton Chirality CD Method) Analytical Chemistry Enantiomer Excess & Absolute Configuration Determination Exciton Chirality CD Method (for Primary Amino Groups)