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1-Decyl-3-methylimidazolium Bis(trifluoromethanesulfonyl)imide. Uses: 1-decyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide is an organic, ionic liquid solvent used in various reactions, such as those with molybdenum(II) complexes with α-diimines, where it helps control chemoselectivity. Group: Battery materials electronic materials. Alternative Names: 3-decyl-1-methyl-1H-Imidazolium salt with 1, ?1, ?1-trifluoro-N-[ (trifluoromethyl) ?sulfonyl]?methanesulfonamide; 1-decyl-3-methyl-1H-Imidazolium salt with 1, 1, 1-trifluoro-N-[ (trifluoromethyl) sulfonyl]methanesulfonamide; 1-Decyl-3-methylimidazolium N,N-bis(trifluoromethylsulfonyl)amide; 1-Decyl-3-methylimidazolium bis(trifluoromethylsulfonyl)amide; 1-Decyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide; 1-Decyl-3-methylimidazolium bis(triflyl)imide; 1-n-Decyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide. CAS No. 433337-23-6. Product ID: bis(trifluoromethylsulfonyl)azanide; 1-decyl-3-methylimidazol-3-ium. Molecular formula: 503.52. Mole weight: C16H27F6N3O4S2. CCCCCCCCCCN1C=C[N+] (=C1)C. C (F) (F) (F)S (=O) (=O)[N-]S (=O) (=O)C (F) (F)F. 1S / C14H27N2. C2F6NO4S2 / c1-3-4-5-6-7-8-9-10-11-16-13-12-15 (2) 14-16; 3-1 (4, 5) 14 (10, 11) 9-15 (12, 13) 2 (6, 7) 8 / h12-14H, 3-11H2, 1-2H3; / q+1; -1. ZYVGZWFCGPUVSH-UHFFFAOYSA-N. >98.0%(T)(HPLC).
1-Octyl-3-methyl-1H-imidazolium bis[(trifluoromethyl)sulfonyl]methane salt
1-Octyl-3-methyl-1H-imidazolium bis[(trifluoromethyl)sulfonyl]methane salt. Uses: Designed for use in research and industrial production. Product Category: Imidazolium Ionic Liquids. CAS No. 916729-96-9. Molecular formula: C15H24F6N2O4S2. Mole weight: 474.48. Purity: ≥99%. Product ID: ACM916729969. Alfa Chemistry ISO 9001:2015 Certified.
Nickel(II) bis(trifluoromethanesulfonimide) hydrate is a compound of utmost importance in the biomedical sector and holds a pivotal role as a catalyst in diverse pharmaceutical procedures. Its catalytic potential enables the synthesis of therapeutics employed for the treatment of neurodegenerative ailments, cancerous conditions, and microbial infections. The exceptional attributes inherent to this compound render it an indispensable constituent in the realm of drug discovery, guaranteeing optimal efficacy and the desired attributes of pharmaceutical agents. Uses: Transition metal catalysts. Synonyms: Nickel, bis[1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl-κO]methanesulfonamidato-κO]-, hydrate (1:x); Nickel bis(trifluoromethylsulfonyl)imide hydrate; Bis[1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl-κO]methanesulfonamidato-κO]nickel hydrate; Bis[bis (trifluoromethylsulfonyl)amino] nickel(II) hydrate. Grades: ≥95%. CAS No. 2067359-93-5. Molecular formula: C4F12N2NiO8S4.xH2O. Mole weight: 618.99 (anhydrous basis).
N,N-Bis(trifluoromethylsulfonyl)aniline. Uses: Designed for use in research and industrial production. Additional or Alternative Names: phenyltrifluoromethanesulfonimide;1,1,1-TRIFLUORO-N-PHENYL-N-[(TRIFLUOROMETHYL)SULFONYL]METHANESULFONAMIDE;N-PHENYLBIS(TRIFLUOROMETHANESULFONIMIDE);N-PHENYLBIS(TRIFLUOROMETHANESULPHONIMIDE);N-PHENYLTRIFLUOROMETHANESULFONIMIDE;N-PHENYLTRIFLUOROMETHANESULPHONIMIDE;N,N-BIS(TRIFLUOROMETHYLSULFONYL)ANILINE;PHENYL TRIFLIMIDE. Product Category: Heterocyclic Organic Compound. CAS No. 37595-74-7. Molecular formula: C8H5F6NO4S2. Mole weight: 357.25. Product ID: ACM37595747. Alfa Chemistry ISO 9001:2015 Certified.
N-Phenyl-bis(trifluoromethanesulfonimide). Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1,1,1-Trifluoro-N-phenyl-N-[(trifluoromethyl)sulfonyl]methanesulfonamide, N,N-Bis(trifluoromethylsulfonyl)aniline, N-Phenyl-trifluoromethanesulfonimide, NSC 240874, Phenyl triflimide. Product Category: Sulfonylation Reagents. CAS No. 37595-74-7. Molecular formula: C8H5F6NO4S2. Mole weight: 357.2422. Purity: 0.97. Product ID: ACM37595747-1. Alfa Chemistry ISO 9001:2015 Certified.
13-{[ (3-tert-Butyloxycarbonyl) -2, 2-dimethyl-4S-phenyl-1, 3-oxazolidin-5R-yl]formyl}-7-O- ( (trifluoromethyl) sulfonyl]oxy) Baccatin III
Intermediate in the synthesis of taxol analogs. Group: Biochemicals. Alternative Names: (4S, 5R) -2, 2-Di methyl -4-phenyl -3, 5-oxazolidinedicarboxyl ic Acid 5-[ (2aR, 4S, 4aS, 6R, 9S, 11S, 12S, 12aR, 12bS) -6, 12b-Bis (acetyloxy) -12- (benzoyloxy) -2a, 3, 4, 4a, 5, 6, 9, 10, 11, 12, 12a, 12b-dodecahydro-11-hydroxy-4a, 8, 13, 13-tetramethyl-5-oxo-4-[[ (trifluoromethyl) sulfonyl]oxy]-7, 11-methano-1H-cyclodeca[3, 4]benz[1, 2-b]oxet-9-yl] 3-(1,1-dimethylethyl) Ester. Grades: Highly Purified. CAS No. 168120-69-2. Pack Sizes: 10mg. US Biological Life Sciences.
Worldwide
A01
A01 is a high affinity Smurf1 E3 ubiquitin ligase inhibitor (Kd = 3.7 nM), which attenuates Smurf1-mediated Smad 1/5 degradation and enhances BMP signaling. Study showed that it potentiated BMP-2-induced osteoblastic activity in C2C12 myoblasts and MC3T3-E1 osteoblast precursor cells. Synonyms: Smurf1-IN-A01; Smurf1INA01; Smurf1 IN A01; Smurf1 inhibitor A01; Smurf1-inhibitor-A01; A01; A 01; A-01; [4-[[4-Chloro-3-(trifluoromethyl)phenyl]sulfonyl]-1-piperazinyl][4-(5-methyl-1H-pyrazol-1-yl)phenyl]methanone; SMURF1 inhibitor A01. Grades: ≥98% by HPLC. CAS No. 1007647-73-5. Molecular formula: C22H20ClF3N4O3S. Mole weight: 512.93.
Dazucorilant
Dazucorilant is a glucocorticoid receptor antagonist. Synonyms: {(4aR)-1-(4-fluorophenyl)-6-[4-(trifluoromethyl)benzene-1-sulfonyl]-1,4,5,6,7,8-hexahydro-4aH-pyrazolo[3,4-g]isoquinolin-4a-yl}(pyridin-2-yl)methanone; (R)-(1-(4-fluorophenyl)-6-((4-(trifluoromethyl)phenyl)sulfonyl)-1,4,5,6,7,8-hexahydro-4aH-pyrazolo[3,4-g]isoquinolin-4a-yl)(pyridin-2-yl)methanone. CAS No. 1496508-34-9. Molecular formula: C29H22F4N4O3S. Mole weight: 582.58.
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