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| Product | Description | |
|---|---|---|
| Cucurbituril | Cucurbituril. Group: Polymers. Alternative Names: CUCURBITURIL; Cucurbituril[6]; 1H, 4H, 14H, 17H-2, 16:3, 15-Dimethano-5H, 6H, 7H, 8H, 9H, 10H, 11H, 12H, 13H, 18H, 19H, 20H, 21H, 22H, 23H, 24H, 25H, 26H-2, 3, 4a, 5a, 6a, 7a, 8a, 9a, 10a, 11a, 12a, 13a, 15, 16, 17a, 18a, 19a, 20a, 21a, 22a, 23a, 24a, 25a, 26a-tetracosaazabispentaleno1, 6:5, 6, 7cyclooct. CAS No. 80262-44-8. Product ID: 3, 5, 8, 10, 13, 15, 18, 20, 23, 25, 28, 30, 31, 33, 35, 37, 41, 43, 45, 47, 49, 51, 53, 55-tetracosazanonadecacyclo[25.3.3.36, 7.311, 12.316, 17.321, 22.22, 31.226, 33.13, 30.15, 8.110, 13.115, 18.120, 23.125, 28.135, 41.137, 55.143, 45.147, 49.151, 53]hexacontane-34, 36, 38, 39, 40, 42, 44, 46, 48, 50, 52, 54-dodecone. Molecular formula: 996.8g/mol. Mole weight: C36H36N24O12. C1N2C3C4N (C2=O)CN5C6C7N (C5=O)CN8C9C2N (C8=O)CN5C8C%10N (C5=O)CN5C%11C%12N (C5=O)CN5C%13C (N1C5=O)N1CN3C (=O)N4CN6C (=O)N7CN9C (=O)N2CN8C (=O)N%10CN%11C (=O)N%12CN%13C1=O. InChI=1S / C36H36N24O12 / c61-25-37-1-38-14-16-42 (26 (38) 62) 4-46-18-20-50 (30 (46) 66) 8-54-22-24-58 (34 (54) 70) 11-57-23-21-53 (33 (57) 69) 7-49-19-17-45 (29 (49) 65) 3-41 (25) 15-13 (37) 39-2-40 (14) 28 (64) 44 (16) 6-48 (18) 32 (68) 52 (20) 10-56 (22) 36 (72) 60 (24) 12-59 (23) 35 (71) 55 (21) 9-51 (19) 31 (67) 47 (17) 5-43 (15) 27 (39) 63 / h13-24H, 1-12H2. MSBXTPRURXJCPF-UHFFFAOYSA-N. |  |
| Cucurbituril | Cucurbituril is a container molecule resembling a hollow pumpkin, with two identical inlets at each end and a hydrophobic cavity in the middle. Cucurbiturils have unique chemical properties that allow them to selectively encapsulate guest molecules such as drugs or catalysts within their cavities, shielding them from the surrounding environment. Cucurbituril has important potential applications in various fields such as drug delivery, catalysis and materials science. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 80262-44-8. Pack Sizes: 100 mg; 250 mg; 1 g. Product ID: HY-W130354. |  |
| Cucurbit[5]uril hydrate | Cucurbiturils are macrocyclic molecules made of glycoluril monomers linked by methylene bridges. The oxygen atoms are located along the edges of the band and are tilted inwards, forming a partly enclosed cavity. Cucurbiturils are commonly written as cucurbit[n]uril, where n is the number of glycoluril units. Two common abbreviations are CB[n], or simply CBn. Uses: Host material for supramolecular chemistry. Group: Hydrophilic polymers. Pack Sizes: Packaging 100 mg in glass insert. Mole weight: C30H30N20O10 · xH2O · xKCl · xHCl. O. Cl. [Cl-]. [K+]. O=C1N2CN3C4C5N (CN6C7C8N (CN9C%10C%11N (CN%12C%13C%14N (CN1C%15C2N%16CN4C (=O) N5CN7C (=O) N8CN%10C (=O) N%11CN%13C (=O) N%14CN%15C%16=O) C%12=O) C9=O) C6=O) C3=O. 1S/C30H30N20O10. 2ClH. K. H2O/c51-21-31-1-32-12-14-36 (22 (32)52)4-40-16-18-44 (26 (40)56)8-48-20-19-47 (29 (48)59)7-43-17-15-39 (25 (43)55)3-35 (21)13-11 (31)33-2-34 (12)24 (54)38 (14)6-42 (16)28 (58)46 (18)10-50 (20)30 (60)49 (19)9-45 (17)27 (57)41 (15)5-37 (13)23 (33)53; ; ; ; /h11-20H, 1-10H2; 2*1H; ; 1H2/q; ; ; +1; /p-1/t11-, 12+, 13+, 14-, 15-, 16+, 17+, 18-, 19-, 20+; ; ;. VIWLZIOPOSWHFW-DVJLYPCZSA-M. | |
| Cucurbit[7]uril hydrate | Cucurbiturils are macrocyclic molecules made of glycoluril monomers linked by methylene bridges. The oxygen atoms are located along the edges of the band and are tilted inwards, forming a partly enclosed cavity. Cucurbiturils are commonly written as cucurbit[n]uril, where n is the number of glycoluril units. Two common abbreviations are CB[n], or simply CBn. Uses: Chemists have used cucurbituril for a variety of applications, including drug delivery, asymmetric synthesis, molecular switching, and dye tuning. Group: Hydrophilic polymers. Pack Sizes: Packaging 100 mg in glass insert. Product ID: 3, 5, 8, 10, 13, 15, 18, 20, 23, 25, 28, 30, 33, 35, 36, 38, 40, 42, 46, 48, 50, 52, 54, 56, 58, 60, 62, 64-octacosazadocosacyclo[30.3.3.36, 7.311, 12.316, 17.321, 22.326, 27.22, 36.231, 38.13, 35.15, 8.110, 13.115, 18.120, 23.125, 28.130, 33.140, 46.142, 64.148, 50.152, 54.156, 58.160, 62]heptacontane-39, 41, 43, 44, 45, 47, 49, 51, 53, 55, 57, 59, 61, 63-tetradecone; hydrate. Molecular formula: 1181g/mol. Mole weight: C42H42N28O14 · xH2O · xHCl. O. Cl. O=C1N2CN3C4C5N (CN6C7C8N (CN9C%10C%11N (CN%12C%13C%14N (CN%15C%16C%17N (CN%18C%19C%20N (CN1C%21C2N%22CN4C (=O) N5CN7C (=O) N8CN%10C (=O) N%11CN%13C (=O) N%14CN%16C (=O) N%17CN%19C (=O) N%20CN%21C%22=O) C%18=O) C%15=O) C%12=O) C9=O) C6=O) C3=O. 1S/C42H42N28O14. ClH. H2O/c71-29-43-1-44-16-18-48 (30 (44)72)4-52-20-22-56 (34 (52)76)8-60-24-26-64 (38 (60)80)12-68-28-27-67 (41 (68 | |
| Cucurbit[8]uril hydrate | Cucurbiturils are macrocyclic molecules made of glycoluril monomers linked by methylene bridges. The oxygen atoms are located along the edges of the band and are tilted inwards, forming a partly enclosed cavity. Cucurbiturils are commonly written as cucurbit[n]uril, where n is the number of glycoluril units. Two common abbreviations are CB[n], or simply CBn. Uses: Chemists have used cucurbituril for a variety of applications, including drug delivery, asymmetric synthesis, molecular switching, and dye tuning. Group: Hydrophilic polymers. Pack Sizes: Packaging 100 mg in glass insert. Product ID: 3, 5, 8, 10, 13, 15, 18, 20, 23, 25, 28, 30, 33, 35, 38, 40, 41, 43, 45, 47, 51, 53, 55, 57, 59, 61, 63, 65, 67, 69, 71, 73-dotriacontazapentacosacyclo[35. 3. 3. 36, 7. 311, 12. 316, 17. 321, 22. 326, 27. 331, 32. 22, 41. 236, 43. 13, 40. 15, 8. 110, 13. 115, 18. 120, 23. 125, 28. 130, 33. 135, 38. 145, 51. 147, 73. 153, 55. 157, 59. 161, 63. 165, 67. 169, 71]octacontane-44, 46, 48, 49, 50, 52, 54, 56, 58, 60, 62, 64, 66, 68, 70, 72-hexadecone; hydrate. Molecular formula: 1347.1g/mol. Mole weight: C48H48N32O16 · xH2O · xHCl. O. Cl. O=C1N2CN3C4C5N (CN6C7C8N (CN9C%10C%11N (CN%12C%13C%14N (CN%15C%16C%17N (CN%18C%19C%20N (CN%21C%22C%23N (CN1C%24C2N%25CN4C (=O) N5CN7C (=O) N8CN%10C (=O) N%11CN%13C (=O) N%14CN%16C (=O) N%17CN%19C (=O) N%20CN%22C (=O) N%23CN%24C%25=O) C%21=O) C%18=O) C%15=O) C%12=O) C9=O) C6=O) C3=O. 1S/C48H48N32O1 | |
| Fuberidazole | Fuberidazole (BAY 33172; Furidazole) is a fungicide. Fuberidazole shows a synergistic effect with cucurbituril (CB) macromolecules, such as CB7 and CB8. Studies have shown that, CB8 induces pK a shifts on Fuberidazole. Fuberidazole significantly inhibits the growth of B. cinerea [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BAY 33172; Furidazole. CAS No. 3878-19-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B1843. | |
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