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  2. [(2R,3R,4S,5S)-3,4,5-triacetyloxy-6-phenylsulfanyloxan-2-yl]methyl acetate

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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

[(2R,3R,4S,5S)-3,4,5-triacetyloxy-6-phenylsulfanyloxan-2-yl]methyl acetate

CC(=O)OCC1OC(Sc2ccccc2)C(C(C1OC(=O)C)OC(=O)C)OC(=O)C Request for Quotation
Chemical Name: [(2R,3R,4S,5S)-3,4,5-triacetyloxy-6-phenylsulfanyloxan-2-yl]methyl acetate
CAS Number: 108032-93-5
Product Number: AG008VQJ(AGN-PC-0001XU)
Synonyms:
MDL No: MFCD01862644
Molecular Formula: C20H24O9S
Molecular Weight: 440.46416

Identification/Properties

Computed Properties
Molecular Weight:
440.463g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
10
Rotatable Bond Count:
11
Exact Mass:
440.114g/mol
Monoisotopic Mass:
440.114g/mol
Topological Polar Surface Area:
140A^2
Heavy Atom Count:
30
Formal Charge:
0
Complexity:
632
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
5
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Phenyl 2,3,4,6-Tetra-O-acetyl-1-thio-α-D-mannopyranoside plays a crucial role in chemical synthesis as a versatile building block for a wide range of organic reactions. Due to its unique structure, this compound is commonly utilized in the preparation of complex carbohydrates and glycoconjugates. Its functional groups enable selective modification, allowing chemists to attach various substituents and create diverse molecular structures. Additionally, Phenyl 2,3,4,6-Tetra-O-acetyl-1-thio-α-D-mannopyranoside serves as a key intermediate in the synthesis of bioactive molecules and pharmaceutical compounds. Its involvement in chemical transformations such as glycosylation reactions makes it a valuable tool in the design and creation of novel organic compounds with potential applications in drug discovery and development.