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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)-

a-L-Galactopyranosyl bromide, 6-deoxy-, triacetate

CC(=O)O[C@H]1[C@H](OC(=O)C)C(C)O[C@H]([C@H]1OC(=O)C)Br Request for Quotation
Chemical Name: a-L-Galactopyranosyl bromide, 6-deoxy-, triacetate
CAS Number: 16741-27-8
Product Number: AG001XDT(AGN-PC-0Q92NE)
Synonyms:
MDL No:
Molecular Formula: C12H17BrO7
Molecular Weight: 353.16318

Identification/Properties

Properties
Form:
Solid
Computed Properties
Molecular Weight:
353.165g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
6
Exact Mass:
352.016g/mol
Monoisotopic Mass:
352.016g/mol
Topological Polar Surface Area:
88.1A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
397
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


Acetobromofucose is a key reagent in chemical synthesis, specifically in organic chemistry. It is commonly used as an intermediate in the synthesis of various complex molecules and natural products. Due to its unique structure and reactivity, acetobromofucose plays a significant role in the modification and functionalization of carbohydrates and other biologically important compounds. Chemists utilize acetobromofucose to introduce bromine and acetate groups into molecules, enabling the creation of diverse chemical derivatives with tailored properties and functionalities. This versatile reagent has found applications in the field of medicinal chemistry, carbohydrate chemistry, and natural product synthesis, allowing researchers to develop novel compounds with potential pharmaceutical and biological activities. By leveraging the reactivity of acetobromofucose, chemists can access a wide range of molecular structures, paving the way for innovative advancements in drug discovery and materials science.