3-CHLORO-1H-INDAZOL-5-AMINE

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CAS:41330-49-8
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CAS:41330-49-8
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3-CHLORO-1H-INDAZOL-5-AMINE manufacturers

3-CHLORO-1H-INDAZOL-5-AMINE Basic information
Product Name:3-CHLORO-1H-INDAZOL-5-AMINE
Synonyms:5-AMINO-3-CHLORO (1H)INDAZOLE;3-Chloro-1H-indazol-5-ylaMine;3-chloro-2H-indazol-5-amine;3-CHLORO-1H-INDAZOL-5-AMINE;5-AMINO-3-CHLOROINDAZOLE;3-Chloro-1H-indazol-5-amine ,97%;107594;1H-Indazol-5-amine, 3-chloro-
CAS:41330-49-8
MF:C7H6ClN3
MW:167.6
EINECS:
Product Categories:
Mol File:41330-49-8.mol
3-CHLORO-1H-INDAZOL-5-AMINE Structure
3-CHLORO-1H-INDAZOL-5-AMINE Chemical Properties
Boiling point 408.7±25.0 °C(Predicted)
density 1.533±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka12.45±0.40(Predicted)
AppearanceLight brown to brown Solid
InChIInChI=1S/C7H6ClN3/c8-7-5-3-4(9)1-2-6(5)10-11-7/h1-3H,9H2,(H,10,11)
InChIKeyCXLAMAWMZAQBKK-UHFFFAOYSA-N
SMILESN1C2=C(C=C(N)C=C2)C(Cl)=N1
Safety Information
Risk Statements 20/21/22
Safety Statements 36/37
HS Code 29339900
MSDS Information
3-CHLORO-1H-INDAZOL-5-AMINE Usage And Synthesis
Chemical PropertiesRed solid
Synthesis
3-CHLORO-5-NITRO-1H-INDAZOLE

4812-45-7

3-CHLORO-1H-INDAZOL-5-AMINE

41330-49-8

The general procedure for the synthesis of 3-chloro-1H-indole-5-aniline using 3-chloro-5-nitro-1H-indazole as starting material was as follows: 1.00 g (5.06 mmol) of 3-chloro-5-nitro-1H-indazole was suspended in 50 mL of ethanol, followed by the addition of 5.71 g (25.3 mmol) of tin chloride dihydrate. The reaction mixture was stirred under reflux conditions overnight. Upon completion of the reaction, saturated aqueous sodium bicarbonate was added to the mixture to neutralize the reaction system, followed by three extractions with ethyl acetate. The organic phases were combined, dried with anhydrous magnesium sulfate and concentrated under reduced pressure to remove the solvent. The resulting crude product was ground with 10% butyl methyl ether and the solid product was collected by filtration. A final 544 mg of the target compound was obtained with a purity of 90% and a yield of 58% of the theoretical value.

References[1] Journal of Chemical Research, Miniprint, 1990, # 11, p. 2601 - 2615
[2] Journal of Medicinal Chemistry, 2003, vol. 46, # 26, p. 5663 - 5673
[3] Patent: US2016/52884, 2016, A1. Location in patent: Paragraph 0649-0652
[4] Patent: KR2015/137095, 2015, A. Location in patent: Paragraph 0867-0870
3-CHLORO-1H-INDAZOL-5-AMINE Preparation Products And Raw materials
Raw materialsAcetic acid-->Sodium nitrite-->Iron-->Calcium hypochlorite-->2-Methyl-4-nitroaniline-->3-CHLORO-5-NITRO-1H-INDAZOLE-->Ethanol
Tag:3-CHLORO-1H-INDAZOL-5-AMINE(41330-49-8) Related Product Information
3-CHLORO-5-NITRO-1H-INDAZOLE 3-CHLORO-1H-INDAZOL-5-AMINE 3-CHLORO-1H-INDAZOLE 3-chloro-1H-indazol-6-amine 5-CHLORO-1H-INDAZOL-3-AMINE 7-chloro-1H-indazol-3-amine 1-METHYL-4-CHLORO-1H-INDAZOL-3-AMINE 4-CHLORO-1H-INDAZOL-3-AMINE 1-(3-CHLORO-5-NITRO-1H-INDAZOL-1-YL)ETHAN-1-ONE 3-CHLORO-4-FLUORO-5-NITRO (1H)INDAZOLE 4-BROMO-3-CHLORO-5-NITRO (1H)INDAZOLE 6-chloro-1H-indazol-3-amine 5-AMINO-4-BROMO-3-CHLORO (1H)INDAZOLE 5-AMINO-3-CHLORO-4-FLUORO (1H)INDAZOLE N-(3-CHLORO-1H-INDAZOL-5-YL)-3,5-BIS(TRIFLUOROMETHYL)BENZENESULFONAMIDE 2,3,3-TRICHLORO-1-(3-CHLORO-5-NITRO-1H-INDAZOL-1-YL)PROP-2-EN-1-ONE 4-CHLORO-N-(3-CHLORO-1H-INDAZOL-5-YL)BENZENESULFONAMIDE

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