Basic Information |
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Product Name: | 3,5-BIS(TRIFLUOROMETHYL)PHENYLBORONIC ACID |
CAS: | 73852-19-4 |
English Synonyms: | ABLOCK AB-13-3572 ; 3,5-BIS(TRIFLUOROMETHYL)BENZENEBORONIC ACID ; 3,5-DI(TRIFLUOROMETHYL)BENZENEBORONIC ACID ; 3,5-DI(TRIFLUOROMETHYL)PHENYLBORONIC ACID ; 3,5-BIS(TRIFLUOROMETHYL)PHENYLBOROIC ACID ; 3,5-BIS(TRIFLUOROMETHYL)PHENYLBORONIC ACID |
MDL Number.: | MFCD00051850 |
H bond acceptor: | 2 |
H bond donor: | 2 |
Smile: | B(c1cc(cc(c1)C(F)(F)F)C(F)(F)F)(O)O |
InChi: | InChI=1S/C8H5BF6O2/c10-7(11,12)4-1-5(8(13,14)15)3-6(2-4)9(16)17/h1-3,16-17H |
InChiKey: | InChIKey=BPTABBGLHGBJQR-UHFFFAOYSA-N |
Property |
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Melting Point: | 217-220 DEG C(LIT)/219-221℃ |
Comments: | APPLICATION: REACTANT INVOLVED IN THE SYNTHESIS OF: METHYLENE-ARYLBUTENONES VIA CARBONYLATIVE ARYLATION OF ALLENOLS. 4-AMINOQUINOLINE ANALOGS VIA ULLMAN / SUZUKI / NEGISHI COUPLING. PRIMARY AMINO ACID DERIVATIVES WITH ANTICONVULSANT ACTIVITY. ALKYL ARYLCARBAMATES VIA CU-CATALYZED COUPLING WITH POTASSIUM CYANATE. ARYL-SUBSTITUTED SUCCINIMIDES AND CYCLIC KETONES BY ASYMMETRIC CONJUGATE ADDITION. AXIALLY CHIRAL DICARBOXYLIC ACIDS FOR ASYMMETRIC MANNICH-TYPE REACTIONS OTHER NOTES: CONTAINS VARYING AMOUNTS OF ANHYDRIDE UNSPSC: 12352103 WGK: 3 |
Safety information |
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WGK Germany: | 3 |
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