| Identification | More | [Name]
2,6-DICHLOROPHENYL ISOTHIOCYANATE | [CAS]
6590-95-0 | [Synonyms]
2,6-DICHLOROPHENYL ISOTHIOCYANATE
1,3-Dichloro-2-isothiocyanatobenzene
2,6-Dichlorophenyl isothiocyanate, 98+% | [EINECS(EC#)]
623-472-5 | [Molecular Formula]
C7H3Cl2NS | [MDL Number]
MFCD00041056 | [Molecular Weight]
204.08 | [MOL File]
6590-95-0.mol |
| Chemical Properties | Back Directory | [Melting point ]
38-42 °C(lit.) | [Boiling point ]
122-124°C 8mm | [density ]
1.37±0.1 g/cm3(Predicted) | [Fp ]
>230 °F
| [storage temp. ]
2-8°C | [form ]
solid | [Sensitive ]
Moisture Sensitive | [BRN ]
639061 | [InChI]
1S/C7H3Cl2NS/c8-5-2-1-3-6(9)7(5)10-4-11/h1-3H | [InChIKey]
SUCGVQHNGIQXGD-UHFFFAOYSA-N | [SMILES]
Clc1cccc(Cl)c1N=C=S | [CAS DataBase Reference]
6590-95-0(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
C | [Risk Statements ]
R34:Causes burns. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . | [RIDADR ]
UN 3261 8/PG 3
| [WGK Germany ]
3
| [HazardClass ]
6.1 | [PackingGroup ]
II | [HS Code ]
2930909899 | [Storage Class]
8A - Combustible corrosive hazardous materials | [Hazard Classifications]
Skin Corr. 1B |
| Hazard Information | Back Directory | [Uses]
2,6-Dichlorophenyl isothiocyanate may be used as a precursor to synthesize 1-(2-aminoethyl)-2-cyano-3-(2,6-dichlorophenyl)guanidine. | [Synthesis Reference(s)]
Tetrahedron Letters, 34, p. 8283, 1993 DOI: 10.1016/S0040-4039(00)61411-9 | [General Description]
2,6-Dichlorophenyl isothiocyanate is an isothiocyanate derivative. It has been synthesized by using 2,6-dichlorobenzaldehyde oxime as a starting reagent. | [Synthesis]
2.00 mmol 2,6-dichlorophenyl dithiocarbamic acid triethylammonium salt was added to a 50 mL aubergine flask, 8.00 mL of acetonitrile, 4.0 mmol of triethylamine were added sequentially, and then stirred at 0°C. During stirring, 1.00 mmol of bis-tribromo 1, |
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