Cas no 39687-22-4 (1,2,3,4-Tetra-O-benzyl-6-O-trityl-b-D-galactopyranose)
39687-22-4 structure
Product Name:1,2,3,4-Tetra-O-benzyl-6-O-trityl-b-D-galactopyranose
CAS No:39687-22-4
MF:C53H50O6
MW:782.960515499115
CID:924819
Update Time:2023-11-22
1,2,3,4-Tetra-O-benzyl-6-O-trityl-b-D-galactopyranose Chemical and Physical Properties
Names and Identifiers
-
- 6-O-Trityl-1,2,3,4-tetra-O-benzyl-β-D-galactopyranose
- 1,2,3,4-Tetra-O-benzyl-6-O-trityl-b-D-galactopyranose
- (2R,3R,4S,5S,6R)-2,3,4,5-Tetrakis(phenylmethoxy)-6-(trityloxymethyl)oxane
-
- Inchi： 1S/C53H50O6/c1-8-22-41(23-9-1)36-54-49-48(40-58-53(45-30-16-5-17-31-45,46-32-18-6-19-33-46)47-34-20-7-21-35-47)59-52(57-39-44-28-14-4-15-29-44)51(56-38-43-26-12-3-13-27-43)50(49)55-37-42-24-10-2-11-25-42/h1-35,48-52H,36-40H2/t48-,49+,50+,51-,52-/m1/s1
- InChI Key： GWEFKLSXFOMSCJ-JGXHNEAVSA-N
- SMILES： O1[C@H]([C@@H]([C@H]([C@H]([C@H]1COC(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)OCC1C=CC=CC=1)OCC1C=CC=CC=1)OCC1C=CC=CC=1)OCC1C=CC=CC=1
Computed Properties
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 6
- Heavy Atom Count: 59
- Rotatable Bond Count: 18
- Complexity: 1080
- Topological Polar Surface Area: 55.4
Experimental Properties
- Density: 1.22±0.1 g/cm3 (20 oC 760 Torr),
- Solubility: Insuluble (4.1E-7 g/L) (25 oC),
1,2,3,4-Tetra-O-benzyl-6-O-trityl-b-D-galactopyranose Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | T207270-1g |
1,2,3,4-Tetra-O-benzyl-6-O-trityl-b-D-galactopyranose |
39687-22-4 | 1g |
$ 590.00 | 2022-06-03 | ||
| TRC | T207270-2.5g |
1,2,3,4-Tetra-O-benzyl-6-O-trityl-b-D-galactopyranose |
39687-22-4 | 2.5g |
$ 950.00 | 2022-06-03 | ||
| TRC | T207270-5g |
1,2,3,4-Tetra-O-benzyl-6-O-trityl-b-D-galactopyranose |
39687-22-4 | 5g |
$ 1950.00 | 2022-06-03 |
1,2,3,4-Tetra-O-benzyl-6-O-trityl-b-D-galactopyranose Related Literature
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Yiding Jiao,Liqun Kang,Jasper Berry-Gair,Kit McColl,Jianwei Li,Haobo Dong,Hao Jiang,Ryan Wang,Furio Corà,Dan J. L. Brett,Ivan P. Parkin J. Mater. Chem. A, 2020,8, 22075-22082
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Albertus D. Handoko,Khoong Hong Khoo,Teck Leong Tan,Hongmei Jin,Zhi Wei Seh J. Mater. Chem. A, 2018,6, 21885-21890
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Saeideh Mirfakhraei,Malak Hekmati,Fereshteh Hosseini Eshbala,Hojat Veisi New J. Chem., 2018,42, 1757-1761
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Yukiya Kitayama Polym. Chem., 2014,5, 2784-2792
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Olga Guselnikova,Gérard Audran,Jean-Patrick Joly,Andrii Trelin,Evgeny V. Tretyakov,Vaclav Svorcik,Oleksiy Lyutakov,Sylvain R. A. Marque Chem. Sci., 2021,12, 4154-4161
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