4-Bromo-1,8-naphthalic anhydride
- Product Name
- 4-Bromo-1,8-naphthalic anhydride
- CAS No.
- 81-86-7
- Chemical Name
- 4-Bromo-1,8-naphthalic anhydride
- Synonyms
- 4-BROMO-1,8-NAPHTHALENEDICARBOXYLIC ANHYDRIDE;4-BROMONAPHTHALIC ANHYDRIDE;4-Bromo-1,8-phthalic anhydride;4-Bromo-1,8-Napthalic Anhydride;4-Bromo-1,8-naphthalic anhydride;4-BroMo-1,8-naphthalic anhydride 95%;4-Bromo-1,8-naphthalic Anhydride >4-Bromo-1,8-Naphthalic Anhydride,>98%;6-BROMO-BENZO[DE]ISOCHROMENE-1,3-DIONE;7-Bromo-1H,3H-naphtho[1,8-cd]pyran-1,3-dione
- CBNumber
- CB8364504
- Molecular Formula
- C12H5BrO3
- Formula Weight
- 277.07
- MOL File
- 81-86-7.mol
4-Bromo-1,8-naphthalic anhydride Property
- Melting point:
- 217-219 °C (lit.)
- Boiling point:
- 467.2±28.0 °C(Predicted)
- Density
- 1.812±0.06 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,Room Temperature
- solubility
- DMSO (Slightly), Methanol (Slightly)
- form
- Solid
- color
- Off-White to Pale Yellow
- InChI
- InChI=1S/C12H5BrO3/c13-9-5-4-8-10-6(9)2-1-3-7(10)11(14)16-12(8)15/h1-5H
- InChIKey
- DTUOTSLAFJCQHN-UHFFFAOYSA-N
- SMILES
- C1(=O)OC(=O)C2=CC=C(Br)C3=C2C1=CC=C3
- CAS DataBase Reference
- 81-86-7(CAS DataBase Reference)
- EPA Substance Registry System
- 1H,3H-Naphtho[1,8-cd]pyran-1,3-dione, 6-bromo- (81-86-7)
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.
N-Bromosuccinimide Price
- Product number
- 324248
- Product name
- 4-Bromo-1,8-naphthalic anhydride
- Purity
- 95%
- Packaging
- 5g
- Price
- $54.53
- Updated
- 2025/07/31
- Product number
- B0858
- Product name
- 4-Bromo-1,8-naphthalic Anhydride
- Purity
- >95.0%(T)
- Packaging
- 5g
- Price
- $45
- Updated
- 2025/07/31
- Product number
- B0858
- Product name
- 4-Bromo-1,8-naphthalic Anhydride
- Purity
- >95.0%(T)
- Packaging
- 25g
- Price
- $155
- Updated
- 2025/07/31
- Product number
- B697930
- Product name
- 4-Bromo-1,8-naphthalic Anhydride
- Packaging
- 500mg
- Price
- $50
- Updated
- 2021/12/16
- Product number
- B697930
- Product name
- 4-Bromo-1,8-naphthalic Anhydride
- Packaging
- 5g
- Price
- $85
- Updated
- 2021/12/16
4-Bromo-1,8-naphthalic anhydride Chemical Properties,Usage,Production
Uses
4-Bromo-1,8-naphthalic Anhydride is used as a starting material in the synthesis of a fluorescent probe for the detection of copper ions in living human LO-2 cell lines.
Synthesis
81-84-5
81-86-7
1. Oxidation: 1,8-Naphthalenedicarboxylic anhydride (2.31 g, 15.0 mmol) was dissolved in acetic acid (60 mL) and sodium dichromate (11.17 g, 40.0 mmol) was added under stirring conditions at room temperature. The suspension was heated to 75 °C and the reaction was carried out for 8 hours. After the reaction was completed, cold water was added to precipitate the product, which was filtered and washed with water to obtain white 1,8-naphthalenedicarboxylic anhydride (2.6 g, 80%, melting point 266-268 °C). 2. Bromination: 1,8-naphthalenedicarboxylic anhydride (1.98 g, 10.0 mmol) was dissolved in aqueous KOH (2.8 g KOH in 12 mL of water), cooled, and bromine was added dropwise. The reaction mixture was heated to 60 °C and kept for 6 h, then acidified with HCl solution. The crude product was obtained by filtration, the solid was dissolved by heating with 5% NaOH solution, filtered and neutralized with HCl solution, filtered again and washed with cold water, and dried to obtain yellow 4-bromo-1,8-naphthalenedicarboxylic anhydride (2.05 g, 82%, melting point 117-119 °C). 3. Condensation: 4-bromo-1,8-naphthalenedicarboxylic anhydride (2.00 g, 5.0 mmol) was refluxed with o-phenylenediamine (0.618 g, 5.0 mmol) in THF for 6 hours. After completion of the reaction (monitored by TLC), the reaction mixture was cooled, filtered and washed with THF to afford brown 3-bromo-benzo[de]benzo[4,5]imidazo[2,1-a]isoquinolin-7-one (2.51 g, 63%, melting point 190-192 °C). Product characterization: 1H NMR (CDCl3 + TFA) δ 8.90 (dd, J=8.48, 0.68 Hz, 1H, ArH), 8.79 (dd, J=7.36, 0.84 Hz, 1H, ArH), 8.53 (d, J=7.92 Hz, 1H, ArH), 8.24 (d, J=7.92 Hz, 1H, ArH), 8.04 (dd, J=7.92 Hz, 1H, ArH), 8.04 (dd, J=7.92 Hz, 1H, ArH), 8.05 (dd, J=7.92 Hz, 1H, ArH). 8.04 (dd, J=8.48, 7.48 Hz, 1H, ArH), 7.74 (m, 3H, ArH), 7.56 (m, 1H, ArH); 13C NMR (CDCl3 + TFA) δ 165.76, 136.55, 134.50, 134.42, 133.44, 131.92, 131.75, 131.68, 131.15, 130.90, 129.30, 128.64, 128.20, 127.26, 124.97, 121.02, 119.98; EIMS m/z: 350 (M+ + 1). Calculated elemental analysis (C18H9BrN2O): C, 61.91; H, 2.60; N, 8.08. Measured values: C, 61.76; H, 2.81; N, 8.45.
References
[1] Chemistry - A European Journal, 2011, vol. 17, # 44, p. 12257 - 12261
[2] European Journal of Medicinal Chemistry, 2013, vol. 68, p. 352 - 360
[3] RSC Advances, 2015, vol. 5, # 52, p. 41803 - 41813
[4] New Journal of Chemistry, 2011, vol. 35, # 8, p. 1690 - 1700
[5] Dyes and Pigments, 2018, vol. 158, p. 353 - 361
4-Bromo-1,8-naphthalic anhydride Preparation Products And Raw materials
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View Lastest Price from 4-Bromo-1,8-naphthalic anhydride manufacturers
- Product
- 4-Bromo-1,8-naphthalic anhydride 81-86-7
- Price
- US $0.00/KG
- Min. Order
- 1KG
- Purity
- 98.2%
- Supply Ability
- 100 tons
- Release date
- 2022-02-18
- Product
- Benzothioxanthene dicarboxylic anhydride 81-86-7
- Price
- US $1.00/KG
- Min. Order
- 1KG
- Purity
- 98%
- Supply Ability
- 1
- Release date
- 2018-08-09