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5-BROMO-1H-INDOLE-3-CARBOXYLIC ACID

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Products Intro: Product Name:5-bromo-1H-indole-3-carboxylic acid
CAS:10406-06-1
Purity:0.95+
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Products Intro: Product Name:5-bromo-1H-indole-3-carboxylic acid
CAS:10406-06-1
Purity:98%(Min,HPLC) Package:1G;1KG;100KG
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Products Intro: Product Name:5-broMo-1H-indole-3-carboxylic acid
CAS:10406-06-1
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Products Intro: Product Name: 5-BROMO-1H-INDOLE-3-CARBOXYLIC ACID
CAS:10406-06-1
Purity:99% Package:1KG;8USD

5-BROMO-1H-INDOLE-3-CARBOXYLIC ACID manufacturers

5-BROMO-1H-INDOLE-3-CARBOXYLIC ACID Basic information
Product Name:5-BROMO-1H-INDOLE-3-CARBOXYLIC ACID
Synonyms:RARECHEM AL BE 0374;5-BroMo-3-indolecarboxylic Acid;1H-Indole-3-carboxylic acid, 5-broMo-;5-BROMOINDOLE-3-CARBOXYLIC ACID;5-BROMO-1H-INDOLE-3-CARBOXYLIC ACID;5-Bromoindole-3-carboxylicAcid>;5-Bromoindole-3-carboxylicacid,97%
CAS:10406-06-1
MF:C9H6BrNO2
MW:240.05
EINECS:
Product Categories:pharmacetical;Indole
Mol File:10406-06-1.mol
5-BROMO-1H-INDOLE-3-CARBOXYLIC ACID Structure
5-BROMO-1H-INDOLE-3-CARBOXYLIC ACID Chemical Properties
Melting point 238-240 °C (decomp)
Boiling point 240°C(lit.)
density 1.838±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form Solid
pka3.68±0.30(Predicted)
color White to Light yellow
InChIInChI=1S/C9H6BrNO2/c10-5-1-2-8-6(3-5)7(4-11-8)9(12)13/h1-4,11H,(H,12,13)
InChIKeyJVZMBSGNSAHFCY-UHFFFAOYSA-N
SMILESN1C2=C(C=C(Br)C=C2)C(C(O)=O)=C1
CAS DataBase Reference10406-06-1(CAS DataBase Reference)
Safety Information
HS Code 2933998090
MSDS Information
5-BROMO-1H-INDOLE-3-CARBOXYLIC ACID Usage And Synthesis
Uses5-Bromo-1H-indole-3-carboxylic Acid is a useful intermediate used in the synthesis of indole derivatives that functions as inhibitors for the vascular endothelial growth factor receptor 2 (VEGFR-2) tyrosine kinase.
Synthesis
5-Bromoindole

10075-50-0

Carbon dioxide

124-38-9

5-BROMO-1H-INDOLE-3-CARBOXYLIC ACID

10406-06-1

Lithium tert-butoxide (LiOtBu, 160 mg, 2.00 mmol) and 5-bromoindole (23.4 mg, 0.4 mmol) were added to a dry two-neck flask. The reaction vessel was evacuated and filled with carbon dioxide gas. Subsequently, N,N-dimethylformamide (DMF, 2 mL) was added and the mixture was stirred and reacted at 100 °C for 24 hours. Upon completion of the reaction, the mixture was cooled to room temperature, the reaction was carefully quenched with 2N hydrochloric acid solution and extracted with ethyl acetate (5 x 5 mL). The organic phases were combined, washed sequentially with water (2 x 5 mL) and saturated saline (1 x 5 mL) and dried over anhydrous magnesium sulfate. The dried organic phases were concentrated under reduced pressure and the residue was purified by preparative thin layer chromatography (Spreader: hexane/acetone=1:1, v/v) to afford the target compound 5-bromo-1H-indole-3-carboxylic acid (153.0 mg, 95% yield) as a white solid.

References[1] Organic Letters, 2012, vol. 14, # 20, p. 5326 - 5329,4
[2] Heterocycles, 2015, vol. 90, # 2, p. 1196 - 1204
5-BROMO-1H-INDOLE-3-CARBOXYLIC ACID Preparation Products And Raw materials
Raw materials5-Bromoindole-->5-Bromoindole-3-carboxaldehyde-->5-BroMo-1H-indole-3-triMethyl ethanone-->Carbon dioxide-->Lithium tert-butoxide-->N,N-Dimethylformamide
Preparation Products5-Chloroindole-3-carboxylic acid
Tag:5-BROMO-1H-INDOLE-3-CARBOXYLIC ACID(10406-06-1) Related Product Information
5-Bromoindole-3-carboxaldehyde 7024 6-BROMO-1H-INDOLE-3-CARBOXYLIC ACID,6-BROMO-1H-INDOLE-3-CARBOXYLIC ACID 4-BROMOINDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER 4-BROMO-1H-INDOLE-2-CARBOXYLIC ACID 4-bromo-1h-indole-3-carboxylic acid 5-BROMO-1H-INDOLE-2-CARBOXYLIC ACID RARECHEM AL BI 0374 5-BROMO-1H-INDOLE-3-CARBOXYLIC ACID METHYL ESTER 6-BROMO-1H-INDOLE-2-CARBOXYLIC ACID METHYL ESTER 7-BROMO-1H-INDOLE-3-CARBOXYLIC ACID 6-BROMO-1H-INDOLE-2-CARBOXYLIC ACID 3-BROMOINDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER Ethyl 6-bromoindole-2-carboxylate 7-BROMO-1H-INDOLE-2-CARBOXYLIC ACID ETHYL ESTER 7-BROMO-1H-INDOLE-2-CARBOXYLIC ACID Ethyl 5-Bromoindole-2-carboxylate 3-BROMO-1H-INDOLE-2-CARBOXYLIC ACID ETHYL ESTER 5-Bromoindole

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