| Weight | 163.245 g/mol |
|---|---|
| Formula | C9H9NS |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
1-Phenylethyl isothiocyanate (32393-32-1, 4478-92-6)
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- Stage and organ dependent effects of 1 Ohexyl2,3,5trimethylhydroquinone, ascorbic acid derivatives, Nheptadecane8,10dione and phenylethyl isothiocyanate in a rat multiorgan carcinogenesis model (International Journal of Cancer, 1998)
- Inhibition of DMBA-initiated rat mammary tumour development by 1-O-hexyl-2,3,5-trimethylhydroquinone, phenylethyl isothiocyanate, and novel synthetic ascorbic acid derivatives (European Journal of Cancer Prevention, 1998)
- (R)-[1-(1-Naphthyl)ethyl] Isothiocyanate and (S)-1-Phenylethyl Isothiocyanate. New Chirality Recognizing Reagents for the Determination of Enantiomeric Purity of Chiral Amines by NMR (Chemistry Letters, 2000)
- Phenylethyl isothiocyanate reverses cisplatin resistance in biliary tract cancer cells via glutathionylation-dependent degradation of Mcl-1 (Oncotarget, 2016)
- ChemInform Abstract: (R)-[1-(1-Naphthyl)ethyl] Isothiocyanate and (S)-1-Phenylethyl Isothiocyanate. New Chirality Recognizing Reagents for the Determination of Enantiomeric Purity of Chiral Amines by NMR. (ChemInform, 2010)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C1=CC=CC=C1)N=C=S
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InChIKeyQQCJPTVZIZVKEZ-UHFFFAOYSA-N
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Alternate Names
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Synthesis
Similar Compounds
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(10137-87-8)
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(3694-45-9)
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(5424-17-9)
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(3173-56-6, 25550-57-6)
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(13203-39-9)
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(74877-10-4)
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2-(1-aminoethyl)phenol hydrochloride
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(41049-53-0)
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1-Phenylethyl isothiocyanate
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