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METHYL 6-BROMO-1H-INDAZOLE-3-CARBOXYLATE

CAS No.
885278-42-2
Chemical Name:
METHYL 6-BROMO-1H-INDAZOLE-3-CARBOXYLATE
Synonyms
6-Bromo-3-(methoxycarbonyl)-1H-indazole;METHYL 6-BROMO-1H-INDAZOLE-3-CARBOXYLATE;6-bromo-1H-indazole-3-carboxylic acid methyl ester;1H-Indazole-3-carboxylic acid, 6-broMo-, Methyl ester
CBNumber:
CB3101481
Molecular Formula:
C9H7BrN2O2
Molecular Weight:
255.07
MDL Number:
MFCD07371573
MOL File:
885278-42-2.mol
MSDS File:
SDS
Last updated:2025-07-24 18:13:51
Product description Number Pack Size Price
Methyl6-bromo-1H-indazole-3-carboxylate OR62001 250mg $73
Methyl 6-bromo-1H-indazole-3-carboxylate 4H23-9-Z7 250mg $80
Methyl6-bromo-1H-indazole-3-carboxylate M12593 500mg $100
Methyl6-bromo-1H-indazole-3-carboxylate M12593 1g $150
Methyl 6-bromo-1H-indazole-3-carboxylate 187688 1g $240

METHYL 6-BROMO-1H-INDAZOLE-3-CARBOXYLATE Properties

Boiling point 399.7±22.0 °C(Predicted)
Density 1.709±0.06 g/cm3(Predicted)
storage temp. 2-8°C(protect from light)
pka 10.71±0.40(Predicted)
Appearance Off-white to pink Solid
InChI InChI=1S/C9H7BrN2O2/c1-14-9(13)8-6-3-2-5(10)4-7(6)11-12-8/h2-4H,1H3,(H,11,12)
InChIKey FIPMZRPZSZXFGK-UHFFFAOYSA-N
SMILES N1C2=C(C=CC(Br)=C2)C(C(OC)=O)=N1

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
HS Code  2933998090

METHYL 6-BROMO-1H-INDAZOLE-3-CARBOXYLATE price More Price(22)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Apolloscientific OR62001 Methyl6-bromo-1H-indazole-3-carboxylate 885278-42-2 250mg $73 2021-12-16 Buy
SynQuest Laboratories 4H23-9-Z7 Methyl 6-bromo-1H-indazole-3-carboxylate 885278-42-2 250mg $80 2021-12-16 Buy
Frontier Specialty Chemicals M12593 Methyl6-bromo-1H-indazole-3-carboxylate 885278-42-2 500mg $100 2021-12-16 Buy
Frontier Specialty Chemicals M12593 Methyl6-bromo-1H-indazole-3-carboxylate 885278-42-2 1g $150 2021-12-16 Buy
Matrix Scientific 187688 Methyl 6-bromo-1H-indazole-3-carboxylate 885278-42-2 1g $240 2021-12-16 Buy
Product number Packaging Price Buy
OR62001 250mg $73 Buy
4H23-9-Z7 250mg $80 Buy
M12593 500mg $100 Buy
M12593 1g $150 Buy
187688 1g $240 Buy

METHYL 6-BROMO-1H-INDAZOLE-3-CARBOXYLATE Chemical Properties,Uses,Production

Chemical Properties

Methyl 6-bromo-1H-indazole-3-carboxylate is an ester compound with a molecular weight of 255.07, a density of 1.709±0.06 g/cm3 and a boiling point of 399.7 °C (760 mm Hg), which is an irritant to the skin and eyes, and is also acutely toxic.

Uses

Methyl 6-bromo-1H-indazole-3-carboxylate is an organic intermediate compound used in chemical and laboratory research, as an organic synthetic material or reaction reagent.It can be used to synthesize its downstream products (Methyl 6-bromo-1-methyl-1H-indazole 3-carboxylate) and other ester compounds.

Synthesis

Methanol

67-56-1

6-BROMO INDAZOLE-3-CARBOXYLIC ACID

660823-36-9

METHYL 6-BROMO-1H-INDAZOLE-3-CARBOXYLATE

885278-42-2

Concentrated sulfuric acid (1.50 mL, 28 mmol) was slowly added to a methanolic (50 mL, 1 mol) suspension of 6-bromo-1H-indazole-3-carboxylic acid (3.00 g, 12 mmol), and the reaction mixture was heated to 90°C and held for 4 hours. After completion of the reaction, it was cooled to room temperature and the mixture was diluted with 200 mL of ethyl acetate and washed sequentially with 150 mL of saturated aqueous sodium bicarbonate and 150 mL of brine. The organic phase was dried with anhydrous sodium sulfate and concentrated under reduced pressure to give 2.42 g (76% yield) of methyl 6-bromo-1H-indazole-3-carboxylate as a yellow solid. The product was dissolved in tetrahydrofuran (50 mL), cooled to 0 °C and sodium hydride (0.417 g, 10.4 mmol) was added in batches. After stirring at 0 °C for 30 min, [β-(trimethylmethylsilyl)ethoxy]methyl chloride (1.85 mL, 10.4 mmol) was added slowly and dropwise. The reaction mixture was slowly warmed to room temperature over 90 min, excess sodium hydride was quenched by the addition of methanol and concentrated under reduced pressure. The residue was diluted with 200 mL of ethyl acetate and washed with 200 mL of brine. The aqueous phase was back-extracted with 50 mL of ethyl acetate, the organic phases were combined, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. Purification by CombiFlash Fast Chromatography System (40g silica gel column; dissolved in dichloromethane; elution gradient: 100:0 to 50:50 heptane:ethyl acetate, 30 min) gave 3.22 g (88% yield) of the target compound as a yellow oil.

References

[1] Patent: WO2013/24011, 2013, A1. Location in patent: Page/Page column 51
[2] Patent: WO2011/50245, 2011, A1. Location in patent: Page/Page column 134-135
[3] Patent: WO2011/20615, 2011, A1. Location in patent: Page/Page column 85; 86

67-56-1
660823-36-9
885278-42-2
Synthesis of METHYL 6-BROMO-1H-INDAZOLE-3-CARBOXYLATE from Methanol and 6-BROMO INDAZOLE-3-CARBOXYLIC ACID

METHYL 6-BROMO-1H-INDAZOLE-3-CARBOXYLATE Preparation Products And Raw materials

Raw materials

Preparation Products

METHYL 6-BROMO-1H-INDAZOLE-3-CARBOXYLATE Suppliers

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METHYL 6-BROMO-1H-INDAZOLE-3-CARBOXYLATE Spectrum

METHYL 6-BROMO-1H-INDAZOLE-3-CARBOXYLATE 6-Bromo-3-(methoxycarbonyl)-1H-indazole 1H-Indazole-3-carboxylic acid, 6-broMo-, Methyl ester 6-bromo-1H-indazole-3-carboxylic acid methyl ester 885278-42-2