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5-BROMO-7-CHLORO-1H-INDAZOLE

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Products Intro: Product Name:5-Bromo-7-chloro-1H-indazole
CAS:635712-44-6
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Products Intro: Product Name:5-Bromo-7-chloro-1H-indazole
CAS:635712-44-6
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Products Intro: Product Name:5-Bromo-7-chloro-1H-indazole
CAS:635712-44-6
Purity:98% HPLC LCMS Package:10G;20G
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Products Intro: Product Name:5-Bromo-7-chloro-1H-indazole
CAS:635712-44-6
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-12718

5-BROMO-7-CHLORO-1H-INDAZOLE manufacturers

5-BROMO-7-CHLORO-1H-INDAZOLE Basic information
Product Name:5-BROMO-7-CHLORO-1H-INDAZOLE
Synonyms:5-BROMO-7-CHLORO-1H-INDAZOLE;1H-Indazole, 5-bromo-7-chloro-
CAS:635712-44-6
MF:C7H4BrClN2
MW:231.48
EINECS:
Product Categories:
Mol File:635712-44-6.mol
5-BROMO-7-CHLORO-1H-INDAZOLE Structure
5-BROMO-7-CHLORO-1H-INDAZOLE Chemical Properties
Melting point ca 205℃
Boiling point 364.1℃ @760mmHg
density 1.878
storage temp. Sealed in dry,Room Temperature
pka10.67±0.40(Predicted)
AppearanceWhite to light yellow Solid
Safety Information
MSDS Information
5-BROMO-7-CHLORO-1H-INDAZOLE Usage And Synthesis
Synthesis
Diazene, 1-(4-bromo-2-chloro-6-methylphenyl)-2-[(1,1-dimethylethyl)thio]-, (1E)-

943145-70-8

5-BROMO-7-CHLORO-1H-INDAZOLE

635712-44-6

In a flame-dried round-bottomed flask, 4-bromo-2-chloro-6-methylphenyl diaza-tert-butyl sulfide (4.60 g, 14.4 mmol) was mixed with potassium tert-butanol (16.1 g, 10 equiv). A stirrer was added and operated under nitrogen atmosphere. Subsequently, anhydrous DMSO (50 mL) was added. The reaction mixture was stirred vigorously for 10 minutes at room temperature. Upon completion of the reaction, the mixture was carefully poured into a mixture consisting of crushed ice (150 mL) and 10% hydrochloric acid (74 mL). The resulting suspension was allowed to stand at 4 °C overnight, after which the solid product was collected by filtration and washed with distilled water. After vacuum drying, 2.86 g of beige solid product (86% yield) was obtained. The product was characterized by 1H-NMR (CDCl3, 500 MHz): δ 7.52 (d, J = 1.5 Hz, 1H), 7.82 (d, J = 1.5 Hz, 1H), 8.08 (s, 1H). Mass spectrometry analysis showed a molecular ion peak (MH+) of 230.90.

References[1] Patent: WO2003/104236, 2003, A1. Location in patent: Page 122
Tag:5-BROMO-7-CHLORO-1H-INDAZOLE(635712-44-6) Related Product Information
5-BROMO-7-CHLORO-1H-INDAZOLE 7-CHLORO-1H-INDAZOLE 4-BroMo-7-chloro-1H-indazole 1H-Indazole, 5,7-dichloro- 7-Bromo-5-chloro-1H-indazole 1,1-Dimethylethyl 5-bromo-7-chloro-1H-indazole-1-carboxylate