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| | 2,2'-Bis(trifluoromethyl)benzidine Basic information |
| Product Name: | 2,2'-Bis(trifluoromethyl)benzidine | | Synonyms: | 2,2'-Bis(trifluoroMethyl)-4,4'-diaMino biphenyl(TFMB/TFDB);2,2'-bis(trifluoromethyl)-[1,1‘-bibiphenyl]-4,4'-diamine;2,2'-bis(trifluoromethyl)-[1,1'-biphenyl]-4,4'-diamine;2,2'-Bis-trifluoromethyl-biphenyl-4,4'-diamine;2,2'-Bis(trifluorome;2,2'-Bis(trifluoroMethyl)-4,4'-diaMino biphenyl (TFMB);TFMB;2,2 '- (trifluoroMethyl) -4,4' - diaMino diphenyl | | CAS: | 341-58-2 | | MF: | C14H10F6N2 | | MW: | 320.23 | | EINECS: | 671-105-2 | | Product Categories: | Biphenyls (for High-Performance Polymer Research);Functional Materials;Reagent for High-Performance Polymer Research;fine chemicals, specialty chemicals, intermediates, electronic chemical, organic synthesis;fine chemicals, specialty chemicals, intermediates, electronic chemical, organic synthesis, functional materials;341-58-2 | | Mol File: | 341-58-2.mol |  |
| | 2,2'-Bis(trifluoromethyl)benzidine Chemical Properties |
| Melting point | 183 °C | | Boiling point | 376.9±42.0 °C(Predicted) | | density | 1.415±0.06 g/cm3(Predicted) | | storage temp. | 2-8°C(protect from light) | | solubility | soluble in Methanol | | pka | 3.23±0.10(Predicted) | | form | powder to crystal | | color | White to Light yellow to Light orange | | InChI | InChI=1S/C14H10F6N2/c15-13(16,17)11-5-7(21)1-3-9(11)10-4-2-8(22)6-12(10)14(18,19)20/h1-6H,21-22H2 | | InChIKey | NVKGJHAQGWCWDI-UHFFFAOYSA-N | | SMILES | C1(C2=CC=C(N)C=C2C(F)(F)F)=CC=C(N)C=C1C(F)(F)F | | CAS DataBase Reference | 341-58-2(CAS DataBase Reference) |
| | 2,2'-Bis(trifluoromethyl)benzidine Usage And Synthesis |
| Uses | 2,2'-Bis(trifluoromethyl)benzidine is used for producing a high strength flexible transparent polyimide material.
| | Synthesis | This 2,2′-bis(trifluoromethyl)-4,4′-dinitrobiphenyl crystal of 42.5 g, toluene of 127.5 g and 5% Pd/C (AER-TYPE: 50% water contained product) of 1.8 g manufactured by N.E. CHEMCAT Corp. were fed in an autoclave made of stainless steel, after the system was replaced sufficiently with hydrogen, pressured with hydrogen for a reaction pressure to be 1 MPa and reaction was carried out at a reaction temperate of 60 °C for 6 hours. After reaction, catalyst was filtered away, toluene in this reaction liquid was distilled away under reduced pressure, concentrated and crystallized, 2,2′-bis(trifluoromethyl)-4,4′-diaminobiphenyl of 28.5 g (purity converted) was obtained by solid-liquid separation. |
| | 2,2'-Bis(trifluoromethyl)benzidine Preparation Products And Raw materials |
| Raw materials | 1,1'-Biphenyl, 4,4'-dinitro-2,2'-bis(trifluoromethyl)-->Hydrazine, 1,2-bis[3-(trifluoromethyl)phenyl]--->[1,1'-Biphenyl]-2,4'-diamine, 2',4-bis(trifluoromethyl)--->Diazene, bis[3-(trifluoromethyl)phenyl]- (9CI)-->2-(Trifluoromethyl)-1-iodo-4-nitrobenzene-->2-Amino-5-nitrobenzotrifluoride-->4-NITRO-2-(TRIFLUOROMETHYL)ACETANILIDE-->2-(TRIFLUOROMETHYL)ACETANILIDE-->3-Nitrobenzotrifluoride |
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