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6-BROMO INDAZOLE-3-CARBOXYLIC ACID

CAS No.
660823-36-9
Chemical Name:
6-BROMO INDAZOLE-3-CARBOXYLIC ACID
Synonyms
6-BroMo-1H-indazole-3-car...;6-Bromo-3-carboxy-1H-indazole;6-broMo-indazole-3-carboxylate;6-BROMO-3-INDAZOLECARBOXYLIC ACID;6-BROMO INDAZOLE-3-CARBOXYLIC ACID;6-Bromo-1H-indazole-3-carboxylicaci;6-Bromo-1H-indazol-3-carboxylic acid;Methyl 6-bromo indazole-3-carboxylate;6-BROMO-1H-INDAZOLE-3-CARBOXYLIC ACID;1H-Indazole-3-carboxylic acid, 6-bromo-
CBNumber:
CB4665676
Molecular Formula:
C8H5BrN2O2
Molecular Weight:
241.04
MDL Number:
MFCD05663977
MOL File:
660823-36-9.mol
Last updated:2025-07-24 18:13:52

6-BROMO INDAZOLE-3-CARBOXYLIC ACID Properties

Boiling point 493.4±25.0 °C(Predicted)
Density 1.946±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka 2.74±0.10(Predicted)
form powder
color wheat

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H317-H319
Precautionary statements  P280-P305+P351+P338
RIDADR  UN2811
HS Code  2933998090

6-BROMO INDAZOLE-3-CARBOXYLIC ACID price More Price(32)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC B683778 6-Bromo-1H-indazole-3-carboxylicAcid 660823-36-9 100mg $50 2021-12-16 Buy
TRC B683778 6-Bromo-1H-indazole-3-carboxylicAcid 660823-36-9 500mg $210 2021-12-16 Buy
AK Scientific W7715 6-Bromoindazole-3-carboxylicacid 660823-36-9 250mg $244 2021-12-16 Buy
SynQuest Laboratories 4H21-9-Z4 6-Bromo-1H-indazole-3-carboxylic acid 96% 660823-36-9 1g $290 2021-12-16 Buy
Biosynth Carbosynth FB11901 6-Bromo-1H-indazole-3-carboxylic acid 660823-36-9 1g $320 2021-12-16 Buy
Product number Packaging Price Buy
B683778 100mg $50 Buy
B683778 500mg $210 Buy
W7715 250mg $244 Buy
4H21-9-Z4 1g $290 Buy
FB11901 1g $320 Buy

6-BROMO INDAZOLE-3-CARBOXYLIC ACID Chemical Properties,Uses,Production

Uses

6-Bromo-1H-indazole-3-carboxylic Acid is used in the synthesis of indazole derivatives as potent hepcidin production inhibitors for the treatment of anemia of chronic diseases (ACD).

Synthesis

6-Bromoisatin

6326-79-0

6-BROMO INDAZOLE-3-CARBOXYLIC ACID

660823-36-9

General procedure for the synthesis of 6-bromoindazole-3-carboxylic acids from 6-bromodihydroindole-2,3-dione: The conversion of substituted indirubic acids to the corresponding indazole-3-carboxylic acids was carried out in essentially the same way as described by Snyder, H.R. et al. This was done as follows: first, the substituted indigo (22.1 mmol) was diluted with 1N sodium hydroxide solution (24 mL) and heated at 50 °C for 30 min. Subsequently, the resulting burgundy-colored solution was cooled to room temperature and kept for 1 hour. Next, the reaction mixture was cooled to 0 °C and treated with an aqueous solution (5.5 mL) of sodium nitrite (22.0 mmol) at 0 °C. The solution was slowly added via a pipette submerged below the surface of a vigorously stirred aqueous solution of sulfuric acid (2.3 mL) (45 mL) at 0°C. The addition process lasted for 15 min, after which the reaction mixture was held for an additional 30 min. Then, a cold (0°C) solution of concentrated hydrochloric acid (20 mL) of tin(II) chloride dihydrate (52.7 mmol) was added to the reaction mixture over a period of 10 minutes and the reaction mixture was held for 60 minutes. Upon completion of the reaction, the precipitated solid was separated by filtration, washed with water and dried to give a quantitative product. The product was of sufficient purity (confirmed by 1H NMR and LC/MS) to be used in the next step without further purification. Alternatively, the acid can be purified by recrystallization from acetic acid to obtain a higher purity substance. The following acids can also be prepared using this method: 6-bromo-1H-indazole-3-carboxylic acid, 5-methoxy-1H-indazole-3-carboxylic acid and 6-methoxy-1H-indazole-3-carboxylic acid.

References

[1] Patent: US2007/78147, 2007, A1. Location in patent: Page/Page column 63
[2] Patent: WO2004/14864, 2004, A1. Location in patent: Page 94
[3] Patent: WO2010/64875, 2010, A2. Location in patent: Page/Page column 17
[4] Patent: WO2011/20615, 2011, A1. Location in patent: Page/Page column 85; 86
[5] Patent: US2012/130069, 2012, A1. Location in patent: Page/Page column 8

6-BROMO INDAZOLE-3-CARBOXYLIC ACID Preparation Products And Raw materials

Global( 141)Suppliers
Supplier Tel Email Country ProdList Advantage
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63687 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49730 58
career henan chemical co
+86-0371-86658258 +8613203830695 factory@coreychem.com China 29802 58
Guangzhou Yuheng Pharmaceutical Technology Co., Ltd
+8613580539051 joe@yuhengpharm.com CHINA 21142 58
KARMEL TECHNOLOGY (HK) CO.,LIMITED
+8618795957998 karmelhk@126.com CHINA 2886 58
Blocksynth Pharmaceutical Technology Co.,Ltd
0086-19817745290; +8619817745290 bd@blocksynth.com China 5661 58
Dayang Chem (Hangzhou) Co.,Ltd.
+86-0571-88938639 +8617705817739 info@dycnchem.com China 52846 58
CR Corporation Limited
+8613062833949 fred.wen@crcorporation.cn China 8647 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418684 +8618949823763 sales@tnjchem.com China 25356 58
Hangzhou MolCore BioPharmatech Co.,Ltd.
+86-057181025280; +8617767106207 sales@molcore.com China 49734 58

View Lastest Price from 6-BROMO INDAZOLE-3-CARBOXYLIC ACID manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
6-BROMO INDAZOLE-3-CARBOXYLIC ACID pictures 2020-01-10 6-BROMO INDAZOLE-3-CARBOXYLIC ACID
660823-36-9
US $1.00 / KG 1KG 99% 100KG Career Henan Chemical Co

6-BROMO INDAZOLE-3-CARBOXYLIC ACID Spectrum

6-BROMO-3-INDAZOLECARBOXYLIC ACID 6-BROMO INDAZOLE-3-CARBOXYLIC ACID 6-BROMO-1H-INDAZOLE-3-CARBOXYLIC ACID 1H-Indazole-3-carboxylic acid, 6-bromo- 6-Bromo-1H-indazol-3-carboxylic acid 6-broMo-indazole-3-carboxylate 6-BroMo-1H-indazole-3-car... 6-Bromo-3-carboxy-1H-indazole Methyl 6-bromo indazole-3-carboxylate 6-Bromo-1H-indazole-3-carboxylicaci 660823-36-9 Building Blocks Indazole API intermediates pharmacetical Indazoles