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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-Allopyranose

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Chemical Name: b-D-Allopyranose
CAS Number: 7283-09-2
Product Number: AG00FBRE(AGN-PC-0U1EZ3)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
180.156g/mol
XLogP3:
-2.6
Hydrogen Bond Donor Count:
5
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
180.063g/mol
Monoisotopic Mass:
180.063g/mol
Topological Polar Surface Area:
110A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
151
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


β-D-Allose is a rare naturally occurring sugar that possesses unique properties making it a valuable component in chemical synthesis. This versatile compound can be utilized in various chemical reactions to yield diverse products. In organic chemistry, β-D-Allose can be employed as a chiral building block for the synthesis of pharmaceuticals, agrochemicals, and other bioactive compounds. Its ability to serve as a precursor for the construction of complex molecules makes it a sought-after reagent in the field of synthetic chemistry.β-D-Allose's distinct structure and reactivity open up a myriad of possibilities for creating novel chemical entities with tailored properties. Additionally, its compatibility with different functional groups and reaction conditions further enhance its utility in organic synthesis, making it an indispensable tool for chemists seeking to develop innovative compounds and materials.