| Weight | 163.201 g/mol |
|---|---|
| Formula | C8H5NOS |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
Benzoyl isothiocyanate (532-55-8)
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- Tridentate ligand formed by the condensation of two benzoyl isothiocyanate molecules in the presence of chlorotris(triphenylphosphine)rhodium. Structure of chlorobis(benzoylisothiocyanate)bis(triphenylphosphine)rhodium-diethyl ether (Inorganic Chemistry, 1976)
- 2,3,4,6-Tetra-O-benzoyl--d-glucopyranosyl isothiocyanate: An efficient reagent for the determination of enantiomeric purities of amino acids, -adrenergic blockers and alkyloxiranes by high-performance liquid chromatography using standard reversed-phase columns (Journal of Chromatography A, 1993)
- Synthesis of guanosine and its derivatives from 5-amino-1-beta-d-ribofuranoxyl-4-imidazolecarboxamide. I. Ring closure with benzoyl isothiocyanate. (Journal of Organic Chemistry, 1967)
- Synthesis of 4H[1,3]Dithiolo[4,5b]pyrroles Through the Reaction of Benzoyl Isothiocyanate and Dialkyl Acetylenedicarboxylates in the Presence of Ph3P. (Tetrahedron Letters, 2006)
- Novel tridentate ligand formed by the condensation of two benzoyl isothiocyanate molecules in the presence of chlorotris(triphenylphosphine)rhodium (Journal of the American Chemical Society, 1975)
- Reactions of per-O-benzoyl--D-Galf isothiocyanate, a chiral resolving agent (Tetrahedron, 1997)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)C(=O)N=C=S
-
InChIKeyCPEKAXYCDKETEN-UHFFFAOYSA-N
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Benzoyl isothiocyanate
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