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5-Bromoisatoic anhydride

Product Name
5-Bromoisatoic anhydride
CAS No.
4692-98-2
Chemical Name
5-Bromoisatoic anhydride
Synonyms
AKOS BBS-00002893;5-Bromoisatoicacid;5-BROMOISATOIC ANHYDRIDE;5-Bromoisoatoic anhydride;5-BromoisatoicAnhydride>5-Bromoisatoic anhydride,97%;5-BROMOISATOIC ANHYDRIDE 90%;5-Bromoisatoic anhydride 95+%;5-Bromoisatoic anhydride, 90% min;5-BROMOISATOIC ANHYDRIDE, TECH., 90%
CBNumber
CB2341787
Molecular Formula
C8H4BrNO3
Formula Weight
242.03
MOL File
4692-98-2.mol
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5-Bromoisatoic anhydride Property

Melting point:
280-285 °C (dec.) (lit.)
Density 
1.826±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
soluble in Dimethylformamide
form 
powder to crystal
pka
9.81±0.20(Predicted)
color 
White to Light yellow to Light orange
CAS DataBase Reference
4692-98-2(CAS DataBase Reference)
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Safety

Hazard Codes 
T,Xi
Risk Statements 
61-20/21-36/37/38
Safety Statements 
53-23-36/37/39-45
WGK Germany 
3
Hazard Note 
Irritant
HazardClass 
IRRITANT, IRRITANT-HARMFUL
HS Code 
29349990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H312Harmful in contact with skin

H315Causes skin irritation

H319Causes serious eye irritation

H332Harmful if inhaled

H335May cause respiratory irritation

H360May damage fertility or the unborn child

Precautionary statements

P201Obtain special instructions before use.

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

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

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.

P308+P313IF exposed or concerned: Get medical advice/attention.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
477702
Product name
5-Bromoisatoic anhydride
Purity
97%
Packaging
5g
Price
$320
Updated
2023/06/20
TCI Chemical
Product number
B3659
Product name
5-Bromoisatoic Anhydride
Purity
>98.0%(HPLC)(T)
Packaging
5g
Price
$134
Updated
2025/07/31
TRC
Product number
B684653
Product name
5-Bromoisatoic anhydride
Packaging
100mg
Price
$75
Updated
2021/12/16
ChemScene
Product number
CS-W017781
Product name
6-Bromo-2H-benzo[d][1,3]oxazine-2,4(1H)-dione
Purity
97.56%
Packaging
25g
Price
$78
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB42908
Product name
5-Bromoisatoic anhydride
Packaging
5G
Price
$100
Updated
2021/12/16
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5-Bromoisatoic anhydride Chemical Properties,Usage,Production

Chemical Properties

Off-white to salmon powder

Uses

5-Bromoisatoic anhydride is an important chemical raw material and pharmaceutical intermediate, mainly used in laboratory research and development processes and chemical production processes.

Preparation

5-Bromoisatoic anhydride is prepared from 5-bromo indole by stirring in a 4:1 mixture of DMF/H2O for 16 h at room temperature.
1HNMR(DMSO-d6): δ 11.85 (s, br., 1H), 7.96 (dd, J = 0.8, 8.7 Hz, 1H), 7.87 (dd, J = 2.3, 8.7 Hz, 1H), 7.09 (dd, J = 8.8, 0.8 Hz, 1H).

Synthesis

87-48-9

4692-98-2

General procedure for the synthesis of 6-bromo-2H-benzo[d][1,3]oxazine-2,4(1H)-dione using 5-bromoindigo red as starting material: 5-bromoindigo red (II) (20.0 g, 88.49 mmol) was uniformly dispersed in dichloromethane (300 mL), and m-chloroperoxybenzoic acid (22.91 g, 132.73 mmol) was added in batches at room temperature. at room temperature. The reaction mixture was stirred at room temperature for 2 h. The reaction progress was monitored by thin layer chromatography (TLC) to confirm the completion of the reaction. Subsequently, the reaction system was cooled to 10°C with continuous stirring and sodium bisulfite solution was slowly added dropwise until the starch potassium iodide paper no longer showed color. The reaction solution was concentrated by rotary evaporation to remove dichloromethane, 50 mL of water was added to mix well with the residue, and then saturated sodium bicarbonate solution was added dropwise until no bubbles were produced. The resulting solid was collected by filtration, washed with a small amount of water and dried at 50 °C to give 20.99 g of 5-bromoisatoindirubic anhydride (III) in 98% yield.

References

[1] Patent: CN106632276, 2017, A. Location in patent: Paragraph 0112; 0113; 0114
[2] Angewandte Chemie, 1980, vol. 92, # 3, p. 196 - 197
[3] Catalysis Science and Technology, 2015, vol. 5, # 10, p. 4830 - 4838
[4] Patent: CN103570726, 2016, B. Location in patent: Paragraph 0085; 0086; 0087
[5] Journal fuer Praktische Chemie (Leipzig), 1886, vol. <2> 33, p. 36

5-Bromoisatoic anhydride Preparation Products And Raw materials

Raw materials

Preparation Products

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5-Bromoisatoic anhydride Suppliers

TCI AMERICA
Tel
800-4238616
Fax
+1-888-520-1075 / +1-503-283-1987
Email
sales@tciamerica.com
Country
Americas
ProdList
23653
Advantage
75
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View Lastest Price from 5-Bromoisatoic anhydride manufacturers

ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
Product
5-Bromo isatoic anhydride 4692-98-2
Price
US $2.20-8.80/kg
Min. Order
1kg
Purity
99%min
Supply Ability
100kg
Release date
2025-08-29
Hefei Lbao Physical & Chemical Science Co.,Ltd
Product
5-Bromoisatoic anhydride 4692-98-2
Price
US $0.00/kg
Min. Order
1kg
Purity
98%
Supply Ability
Customise
Release date
2025-08-19
Hebei Chuanghai Biotechnology Co., Ltd
Product
5-Bromoisatoic anhydride 4692-98-2
Price
US $8.90/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 mt
Release date
2024-11-28

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