Weight | 116.189 g/mol |
---|---|
Formula | C4H8N2S |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 2 |
ALLYLTHIOUREA (109-57-9)
thiosinamine
Score:
#6 in Optics
,
#1565 in Physics
,
#4705 in Chemistry
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- Estimation of Nitrifying Bacterial Activities by Measuring Oxygen Uptake in the Presence of the Metabolic Inhibitors Allylthiourea and Azide (Applied and Environmental Microbiology, 1998)
- Measurement of nitrification rates in lake sediments: Comparison of the nitrification inhibitors nitrapyrin and allylthiourea (Microbial Ecology, 1984)
- The quality and performance of the organometallic complex nonlinear optical material tri-allylthiourea cadmium chloride (ATCC) (Journal of Crystal Growth, 1990)
- The preparation and characterization of a new organometallic nonlinear optical material Tri-allylthiourea mercury bromide (ATMB) crystal (Materials Research Bulletin, 1993)
- Gold recovery onto poly(acrylamide-allylthiourea) hydrogels synthesized by treating with gamma radiation (Analytica Chimica Acta, 2005)
- A novel metal-organic coordination complex crystal: tri-allylthiourea zinc chloride (ATZC) (Crystal Research and Technology, 2005)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - thiosinamine
-
SMILESC=CCNC(=S)N
-
InChIKeyHTKFORQRBXIQHD-UHFFFAOYSA-N
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Synthesis
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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