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Weight172.297 g/mol
FormulaC8H16N2S
Hydrogen Acceptors1
Hydrogen Donors1
Aromatic Rings0
Rotatable Bonds4

21645-26-1 (21645-26-1)

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Alternate Names

  • SMILES
    CCN(CC)C(=S)NCC=C
  • InChIKey
    QADMBPYDNAHONY-UHFFFAOYSA-N

External Links

Synthesis

1,1-diethylthiourea  +  ALLYL CHLORIDE (Alkylation of primary amines)
Reactant  +  1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide (Nicolaou IBX dehydrogenation)
Synthesis of 21645-26-1 ›

Similar Compounds

1,1-diethylthiourea (26914-14-7)
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ALLYLTHIOUREA (109-57-9)
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1,3-Diethyl-2-thiourea (105-55-5)
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pyrrolidine-1-carbothioamide (40398-36-5)
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1-Piperidinethiocarboxamide (14294-09-8)
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morpholine-4-carbothioamide (14294-10-1)
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4-Allylthiosemicarbazide (3766-55-0)
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Azepane-1-carbothioamide (68881-66-3)
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1,3-Diisopropylthiourea (2986-17-6)
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TRIMETHYLTHIOUREA (2489-77-2)
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TETRAMETHYLTHIOUREA (2782-91-4)
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1,3-Di-tert-butylthiourea (4041-95-6)
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1,3-Dibutylthiourea (109-46-6)
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Diisobutyl thiourea (29214-81-1)
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Propylenethiourea (2055-46-1)
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2-Imidazolidinethione (96-45-7)
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Dimorpholinomethane (5625-90-1)
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N,N'-dihexylthiourea (21071-28-3)
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1-Acetyl-2-thiohydantoin (584-26-9)
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26957-73-3 (26957-73-3)
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1,3-Diallylurea (1801-72-5)
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4-Ethyl-3-thiosemicarbazide (13431-34-0)
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N-Isopropylthiourea (1719-76-2)
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88-11-9 (88-11-9)
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N,N-Dimethylthiourea (6972-05-0)
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102353-42-4 (102353-42-4)
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N'-Benzoyl-N,N-diethylthiourea (58328-36-2)
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SODIUM DIETHYLDITHIOCARBAMATE (148-18-5)
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tert-butylthiourea (7204-48-0)
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N,N'-METHYLENEBISACRYLAMIDE (110-26-9)
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1-Butyl-2-thiourea (1516-32-1)
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N,N-Diethylallylamine (5666-17-1)
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13431-39-5 (13431-39-5)
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1-isopropylimidazolidin-2-one (21921-33-5)
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N-Acetylthiourea (591-08-2)
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1-Hexyl-2-thiourea (21071-27-2)
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32813-48-2 (32813-48-2)
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77644-45-2 (77644-45-2)
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7398-69-8 (26062-79-3, 7398-69-8)
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1,3-Dimethylthiourea (61805-96-7, 534-13-4)
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1,1-Diethylguanidine Sulfate (54259-07-3)
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5807-14-7 (5807-14-7)
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84030-20-6 (84030-20-6)
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