
CAS 183875-28-7
:Formula:C35H36O6S
InChI:InChI=1S/C35H36O6S/c1-26(36)40-34-33(39-24-29-18-10-4-11-19-29)32(38-23-28-16-8-3-9-17-28)31(25-37-22-27-14-6-2-7-15-27)41-35(34)42-30-20-12-5-13-21-30/h2-21,31-35H,22-25H2,1H3/t31-,32+,33+,34-,35+/m1/s1
InChI key:IKFDEPUTIUTSLC-NVCPMKERSA-N
SMILES:CC(=O)O[C@@H]1[C@H]([C@H]([C@H](O[C@H]1SC2=CC=CC=C2)COCC3=CC=CC=C3)OCC4=CC=CC=C4)OCC5=CC=CC=C5
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Phenyl 2-O-Acetyl-3,4,6-tri-O-benzyl-1-thio-beta-D-galactopyranoside
CAS:Formula:C35H36O6SPurezza:min. 98.0 area%(HPLC)Colore e forma:White to Almost white powder to crystalPeso molecolare:584.73Phenyl 2-O-Acetyl-3,4,6-tri-O-benzyl-1-thio-β-D-galactopyranoside
CAS:Phenyl 2-O-Acetyl-3,4,6-tri-O-benzyl-1-thio-β-D-galactopyranosideFormula:C35H36O6SPurezza:≥95%Peso molecolare:584.73Phenyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-b-D-galactopyranoside
CAS:Phenyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-b-D-galactopyranoside is a biochemical reagent utilized in glycoscience research. Glycoscience examines the structure, synthesis, biology, and evolution of sugars, covering carbohydrate chemistry, glycoconjugate formation and degradation, protein-glycan recognition, and the roles of glycans in biological systems. This field has strong connections to fundamental research, biomedicine, and biotechnology.Formula:C35H36O6SPeso molecolare:584.72Phenyl 2-O-Acetyl-3,4,6-tri-O-benzyl-1-thio-b-D-galactopyranoside
CAS:Phenyl 2-O-Acetyl-3,4,6-tri-O-benzyl-1-thio-b-D-galactopyranoside is a glycosylated sugar that is under custom synthesis. The molecule contains a fluorinated benzene ring and an acetyl group. Phenyl 2-O-Acetyl-3,4,6-tri-O-benzyl 1,5 b -D -galactopyranoside can be modified in the laboratory to produce different derivatives and modifications. This product is made of high purity and has CAS No. 18387528 7.Formula:C35H36O6SPurezza:Min. 95%Peso molecolare:584.72 g/mol





