| Identification | Back Directory | [Name]
2,4-BIS(P-TOLYLTHIO)-1,3-DITHIA-2,4-DIPHOSPHETANE-2,4-DISULFIDE | [CAS]
114234-09-2 | [Synonyms]
ERK
EK5
Hek5
Qek2
Sek3
Cek5
DR-T
Tyro5
EPHB2
EPHT3
EPH receptor B2
EphB2 active human
Sulfuratingreagent
Heimgartner reagent
HEIMAGARTNER REAGENT
DAVY-REAGENT P-TOLYL
Human EPHB2 Protein, His Tag
Human EPHB2 Protein, Fc & His Tag
Human EPHB2 Protein, His & GST Tag
ANTI-EPHB2 antibody produced in mouse
Tyrosine-protein kinase receptor EPH-2
Recombinant Human EPHB2 Protein, Fc Tag
EPHB2 (570-end), active, GST tagged human
ELK/ Tyrosine-protein kinase receptor EPH-3
Monoclonal Anti-EPHB2 antibody produced in mouse
2,4-Bis(p-tolythio)-1,3-dithia-2,4-diphosphetane-2,4-disulfide
2,4-BIS(P-TOLYLTHIO)-1,3,2,4-DITHIADIPHOSPHETANE 2,4-DISULFIDE
2,4-BIS(P-TOLYLTHIO)-1,3-DITHIA-2,4-DIPHOSPHETANE-2,4-DISULFIDE
2,4-Bis(p-tolylthio)-1,3-dithia-2,4-diphosphetane 2,4-Disulfide
1,3,2,4-Dithiadiphosphetane, 2,4-bis[(4-methylphenyl)thio]-, 2,4-disulfide
2,4-BIS(P-TOLYLTHIO)-1,3-DITHIA-2,4-DIPHOSPHETANE-2,4-DISULFIDE [SULFURATING REAGENT]
2,4-Bis(p-tolylthio)-1,3,2,4-dithiadiphosphetane 2,4-disulfide, DR-T, Heimgartner reagent
2,4-bis[(4-methylphenyl)sulfanyl]-2,4-bis(sulfanylidene)-1,3,2λsup5sup,4λsup5sup-dithiadiphosphetane
2-({2,4-bis[(4-Methylphenyl)sulfanyl]-1,3,2$l^{5},4-dithiadiphosphetan-2-yl}disulfanyl)-2,4-bis[(4-Methylphenyl)sulfanyl]-1,3,2$l^{5},4-dithiadiphosphetane | [Molecular Formula]
C14H14P2S6 | [MDL Number]
MFCD00059044 | [MOL File]
114234-09-2.mol | [Molecular Weight]
436.6 |
| Chemical Properties | Back Directory | [Melting point ]
209-213 °C (dec.)
| [Boiling point ]
566.2±53.0 °C(Predicted) | [density ]
1.52±0.1 g/cm3(Predicted) | [storage temp. ]
-20°C | [solubility ]
Chloroform (Slightly, Heated), DMSO (Sparingly, Heated) | [form ]
Solid | [color ]
Pale Yellow to Light Yellow | [biological source]
mouse | [BRN ]
7222715 |
| Hazard Information | Back Directory | [Uses]
2,4-Bis(p-tolylthio)-1,3-dithia-2,4-diphosphetane-2,4-disulfide is used in preparation of (Cyclohexyl)pyridine Carboxamides as herbicides. | [Purification Methods]
Recrystallise it from toluene (light yellow solid), wash it with Et2O and dry in vacuo. [Jennt & Heimgarter Helv Chim Acta 70 1001 1987.] |
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