5,6-DIHYDRO-4H-CYCLOPENTATHIAZOL-2-YLAMINE

5,6-DIHYDRO-4H-CYCLOPENTATHIAZOL-2-YLAMINE Suppliers list
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Products Intro: Product Name:2-Amino-5,6-dihydro-4H-cyclopenta[d]thiazole
CAS:53051-97-1
Purity:>=95% Package:0.1g;0.25g;1g;5g;10g
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Products Intro: Product Name:5,6-Dihydro-4H-cyclopenta[d]thiazol-2-amine
CAS:53051-97-1
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-47703
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Products Intro: Product Name:5,6-Dihydro-4H-cyclopentathiazol-2-ylamine
CAS:53051-97-1
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Products Intro: Product Name:5,6-dihydro-4h-cyclopentathiazol-2-ylamine
CAS:53051-97-1
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Products Intro: Product Name:5,6-DIHYDRO-4H-CYCLOPENTATHIAZOL-2-YLAMINE
CAS:53051-97-1
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5,6-DIHYDRO-4H-CYCLOPENTATHIAZOL-2-YLAMINE manufacturers

5,6-DIHYDRO-4H-CYCLOPENTATHIAZOL-2-YLAMINE Basic information
Product Name:5,6-DIHYDRO-4H-CYCLOPENTATHIAZOL-2-YLAMINE
Synonyms:5,6-DIHYDRO-4H-CYCLOPENTATHIAZOL-2-YLAMINE;AKOS BB-9240;AKOS BBS-00002729;TIMTEC-BB SBB005653;5,6-Dihydro-4H-cyclopentathiazol-2-ylaMinehydrobroMide;5,6-dihydro-4H-cyclopenta[d]thiazol-2-aMine hydrobroMide;5,6-DIHYDRO-4H-CYCLOPENTA[D]THIAZOL-2-AMINE;2-Amino-5,6-dihydro-4H-cyclopenta[d]thiazole
CAS:53051-97-1
MF:C6H8N2S
MW:140.21
EINECS:
Product Categories:
Mol File:53051-97-1.mol
5,6-DIHYDRO-4H-CYCLOPENTATHIAZOL-2-YLAMINE Structure
5,6-DIHYDRO-4H-CYCLOPENTATHIAZOL-2-YLAMINE Chemical Properties
Melting point 96-99°C
Boiling point 295.5±9.0 °C(Predicted)
density 1.354±0.06 g/cm3(Predicted)
storage temp. 2-8°C(protect from light)
pka6.02±0.20(Predicted)
Safety Information
HS Code 2934999090
MSDS Information
5,6-DIHYDRO-4H-CYCLOPENTATHIAZOL-2-YLAMINE Usage And Synthesis
Synthesis
2-Amino-5,6-dihydro-4H-cyclopentathiazole hydrochloride

82514-58-7

5,6-DIHYDRO-4H-CYCLOPENTATHIAZOL-2-YLAMINE

53051-97-1

General procedure for the synthesis of 5,6-dihydro-4H-cyclopentathiazol-2-amines from 2-amino-5,6-dihydro-4H-cyclopentathiazole hydrochloride: 1. 2-Amino-5,6-dihydro-4H-cyclopentathiazole hydrochloride (16.5 g, 93 mmol) was added to a mixture of aqueous sodium bicarbonate (16.5 g dissolved in 250 mL of water) and 25% THF/EtOAc (160 mL, v/v). 2. The reaction mixture was stirred at room temperature for 15 minutes. 3. The mixture was filtered through a diatomaceous earth pad to clarify the mixture. 4. The organic layer was separated and dried over anhydrous magnesium sulfate and subsequently concentrated under vacuum to 47 g. The mixture was purified by adding toluene (100 mL). 5. Toluene (100 mL) was added and the mixture was again concentrated to 45 g under vacuum. 6. the mixture was diluted with heptane (40 mL), cooled and the product was collected by filtration and dried to afford 5,6-dihydro-4H-cyclopentathiazol-2-amine as the free base (10.75 g, 85% yield). Product characterization data: 1H NMR (CD3OD) δ 4.88 (2H, s), 2.75-2.70 (2H, m), 2.60-2.55 (2H, m), 2.39-2.33 (2H, m).

References[1] Patent: US2007/149499, 2007, A1. Location in patent: Page/Page column 19
Tag:5,6-DIHYDRO-4H-CYCLOPENTATHIAZOL-2-YLAMINE(53051-97-1) Related Product Information
5,6-DIHYDRO-4H-CYCLOPENTA[B]THIOPHENE-2-CARBOXYLIC ACID 7H-CYCLOPENTA[B]PYRIDIN-7-ONE, 5,6-DIHYDRO- N-cyclopropyl-5,6-dihydro-4H-cyclopenta[d][1,3]thiazol-2-amine 5,6-DIHYDRO-4H-CYCLOPENTATHIAZOL-2-YLAMINE 2-Amino-5,6-dihydro-4H-cyclopentathiazole hydrochloride N-methyl-5,6-dihydro-4H-cyclopenta[d][1,3]thiazol-2-amine ZERENEX E/5030002