Other grades of this product :
| N-Phenyl-bis(trifluoromethanesulfonimide) Basic information |
| Product Name: | N-Phenyl-bis(trifluoromethanesulfonimide) | | Synonyms: | phenyltrifluoromethanesulfonimide;N-PHENYLBIS(TRIFLUOROMETHANESULFONIMIDE);N-PHENYLBIS(TRIFLUOROMETHANESULPHONIMIDE);N-PHENYLTRIFLUOROMETHANESULFONIMIDE;N-PHENYLTRIFLUOROMETHANESULPHONIMIDE;N,N-BIS(TRIFLUOROMETHYLSULFONYL)ANILINE;1,1,1-TRIFLUORO-N-PHENYL-N-[(TRIFLUOROMETHYL)SULFONYL]METHANESULFONAMIDE;N-Phenylbis(trifluoromethanesulphonimide), Phenyl triflimide | | CAS: | 37595-74-7 | | MF: | C8H5F6NO4S2 | | MW: | 357.25 | | EINECS: | 609-445-0 | | Product Categories: | API intermediates | | Mol File: | 37595-74-7.mol |
| N-Phenyl-bis(trifluoromethanesulfonimide) Chemical Properties |
| Melting point | 100-102 °C(lit.) | | Boiling point | 305.3±52.0 °C(Predicted) | | density | 1.766±0.06 g/cm3(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | Soluble in methanol. Slightly soluble in chloroform and ethyl acetate. | | form | Crystals or Crystalline Powder | | pka | -13.12±0.50(Predicted) | | color | White or colorless | | Sensitive | Moisture Sensitive | | BRN | 1269141 | | Stability: | Moisture Sensitive | | InChIKey | DIOHEXPTUTVCNX-UHFFFAOYSA-N | | CAS DataBase Reference | 37595-74-7(CAS DataBase Reference) | | NIST Chemistry Reference | N-phenyltrifluoromethanesulfonimide(37595-74-7) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 3 | | F | 21 | | TSCA | No | | HazardClass | IRRITANT | | HS Code | 29242100 |
| N-Phenyl-bis(trifluoromethanesulfonimide) Usage And Synthesis |
| Chemical Properties | white to off-white crystalline powder | | Uses | N-Phenylbis(trifluoromethanesulfonamide) is used in the enantioselective synthesis of β-amino acids via the Mannich reaction. Used in the synthesis of sphingosine 1-phosphate-1 receptor agonists usefu
l in pharmaceutical application. | | Uses | N-Phenylbis(trifluoromethanesulfonamide) is used in the enantioselective synthesis of β-amino acids via the Mannich reaction. Used in the synthesis of sphingosine 1-phosphate-1 receptor agonists useful in pharmaceutical application. | | Uses | Acts as a transparent strong electron-withdrawing p-type dopant in carbon nanotubesReactant for: Synthesis of amphoteric alpha-boryl aldehydes Enantioselective synthesis of core ring skeleton of leucosceptroids A-D Stereoselective synthesis of monoamine reuptake inhibitor NS9544 acetate Stereoselective sulfoxidation |
| N-Phenyl-bis(trifluoromethanesulfonimide) Preparation Products And Raw materials |
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