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2,3-Naphthalenedicarboxylic Anhydride

Appearance
Product Name
2,3-Naphthalenedicarboxylic Anhydride
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
Formula Weight
198.17
MOL File
716-39-2.mol
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2,3-Naphthalenedicarboxylic Anhydride Property

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)
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Safety

Safety Statements 
22-24/25
HS Code 
2917.39.7000
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H332Harmful if inhaled

H335May cause respiratory irritation

Precautionary statements

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

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

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
S876682
Product name
2,3-NAPHTHALIC ANHYDRIDE
Purity
Aldrich
Packaging
50mg
Price
$110
Updated
2024/03/01
TCI Chemical
Product number
N0530
Product name
2,3-Naphthalenedicarboxylic Anhydride
Purity
>95.0%(GC)(T)
Packaging
25g
Price
$192
Updated
2024/03/01
TCI Chemical
Product number
N0530
Product name
2,3-Naphthalenedicarboxylic Anhydride
Purity
>95.0%(GC)(T)
Packaging
250g
Price
$772
Updated
2024/03/01
TRC
Product number
N363000
Product name
2,3-NAPHTHALIC ANHYDRIDE
Packaging
5g
Price
$100
Updated
2021/12/16
TRC
Product number
N363000
Product name
2,3-NAPHTHALIC ANHYDRIDE
Packaging
1g
Price
$80
Updated
2021/12/16
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2,3-Naphthalenedicarboxylic Anhydride Chemical Properties,Usage,Production

Appearance

2,3-NAPHTHALENEDICARBOXYLIC ANHYDRIDE is a pale Beige Solid.

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 Preparation Products And Raw materials

Raw materials

Preparation Products

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2,3-Naphthalenedicarboxylic Anhydride Suppliers

Nanjing Xinmeihe Pharmaceutical Co., Ltd.
Tel
025-57672321 13739186949
Fax
025-57672123
Email
2548785915@qq.com
Country
China
ProdList
281
Advantage
58
Zhangjiakou Siruikai Technology Co., LTD
Tel
0313-5020135 15831567206
Email
zhaoy@sirichem.com
Country
China
ProdList
58
Advantage
58
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44688
Advantage
61
Puyang Huicheng Electronic Material Co. Ltd.
Tel
0393-0393-0393-8910800 15039333257
Fax
0393-8912775
Email
info@huichengchem.com
Country
China
ProdList
557
Advantage
64
Shanghai Longsheng chemical Co.,Ltd.
Tel
021-58099652-8005 13585536065
Fax
021-58099609
Email
bin.wu@shlschem.com
Country
China
ProdList
9809
Advantage
59
Shandong Xiya Chemical Co., Ltd
Tel
4009903999 13355009207
Fax
0539-6365991
Email
3007715519@qq.com
Country
China
ProdList
18738
Advantage
57
Maya High Purity Chemicals
Tel
+86 (573) 82222445 (0)18006601000 452520369
Fax
+86 (573) 82222643
Email
sales@maya-r.com
Country
China
ProdList
11707
Advantage
57
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View Lastest Price from 2,3-Naphthalenedicarboxylic Anhydride manufacturers

Career Henan Chemical Co
Product
2,3-NAPHTHALENEDICARBOXYLIC ANHYDRIDE 716-39-2
Price
US $2.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
ask
Release date
2018-12-20

716-39-2, 2,3-Naphthalenedicarboxylic AnhydrideRelated Search:


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  • 2,3-NAPHTHALENEDICARBOXYLIC ANHYDRIDE ISO 9001:2015 REACH
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  • Exciton Chirality CD Method (for Primary Amino Groups)
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  • Absolute Conefiguration Determination (Exciton Chirality CD Method)
  • Absolute Configuration Determination (Exciton Chirality CD Method)
  • Analytical Chemistry
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