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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)-

b-D-Galactopyranoside, 2-nitrophenyl 1-thio-

OC[C@H]1O[C@@H](Sc2ccccc2[N+](=O)[O-])[C@@H]([C@H]([C@H]1O)O)O Request for Quotation
Chemical Name: b-D-Galactopyranoside, 2-nitrophenyl 1-thio-
CAS Number: 1158-17-4
Product Number: AG000GWC(AGN-PC-0P86AV)
Synonyms:
MDL No:
Molecular Formula: C12H15NO7S
Molecular Weight: 317.3150

Identification/Properties

Computed Properties
Molecular Weight:
317.312g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
3
Exact Mass:
317.057g/mol
Monoisotopic Mass:
317.057g/mol
Topological Polar Surface Area:
161A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
366
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P233-P260-P261-P264-P270-P271-P280-P301+P312-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P330-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (2R,3R,4S,5R,6S)-2-(Hydroxymethyl)-6-((2-nitrophenyl)thio)tetrahydro-2H-pyran-3,4,5-triol is commonly utilized in chemical synthesis as a versatile building block. Its unique structure containing multiple functional groups makes it a valuable intermediate in the preparation of various complex compounds. In organic synthesis, this compound can be selectively modified at different sites to introduce diverse functionalities, enabling the creation of structurally diverse molecules. Its hydroxymethyl group can participate in various reactions such as protection, oxidation, or reduction, while the nitrophenylthio moiety offers opportunities for further derivatization through substitution or elimination reactions. Overall, the compound's stereochemistry and functional groups make it a valuable tool for designing and constructing novel molecules in chemical synthesis.