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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)-

Acarbose D-Fructose Impurity

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Chemical Name: Acarbose D-Fructose Impurity
CAS Number: 1013621-79-8
Product Number: AG008WZP(AGN-PC-0WBNBZ)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
1192.089g/mol
XLogP3:
-1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
32
Rotatable Bond Count:
35
Exact Mass:
1191.385g/mol
Monoisotopic Mass:
1191.385g/mol
Topological Polar Surface Area:
400A^2
Heavy Atom Count:
83
Formal Charge:
0
Complexity:
2460
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
19
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


Acarbose D-Fructose Impurity is commonly utilized in chemical synthesis as a reagent for the production of pharmaceuticals and fine chemicals. Its presence in a reaction mixture can influence the overall yield and selectivity of the desired product. Furthermore, Acarbose D-Fructose Impurity can act as a chiral auxiliary, imparting asymmetry to the synthesized compounds. This impurity plays a crucial role in the synthesis of various organic molecules, including carbohydrates, amino acids, and natural products, by participating in key bond-forming and stereochemical-determining steps. Its ability to enhance the efficiency and specificity of chemical reactions makes it a valuable tool in the hands of synthetic chemists striving to access complex molecules with high levels of structural precision.