1. Home
  2. D-Galactose, 2-deoxy-2-fluoro-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

D-Galactose, 2-deoxy-2-fluoro-

OC[C@H]([C@@H]([C@@H]([C@H](C=O)F)O)O)O Request for Quotation
Chemical Name: D-Galactose, 2-deoxy-2-fluoro-
CAS Number: 51146-53-3
Product Number: AG01CBEA(AGN-PC-0OBGN7)
Synonyms:
MDL No:
Molecular Formula: C6H11FO5
Molecular Weight: 182.1469432

Identification/Properties

Properties
MP:
130-135°C
Storage:
-10 ℃;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
182.147g/mol
XLogP3:
-2.4
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
5
Exact Mass:
182.059g/mol
Monoisotopic Mass:
182.059g/mol
Topological Polar Surface Area:
98A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
142
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
4
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

Request for Quotation

Customer Feedback

Chemical Structure


2-Deoxy-2-fluoro-D-galactose, also known as $name$, plays a crucial role in chemical synthesis. This compound is widely utilized as a building block in the creation of various organic molecules, particularly in carbohydrate chemistry. Its unique structure, featuring a fluorine substitution at the 2-position and a deoxy sugar configuration, imparts specific properties that are valuable for designing novel compounds.In chemical synthesis, 2-Deoxy-2-fluoro-D-galactose serves as a key precursor for the production of specialized sugars, glycosides, and glycoconjugates. Its presence in the molecule can influence the reactivity and selectivity of reactions, leading to the formation of desired stereoisomers and regioisomers. Moreover, the fluoro substituent in 2-Deoxy-2-fluoro-D-galactose can introduce unique properties such as altered hydrophobicity and enhanced metabolic stability in the synthesized compounds.Researchers and chemists leverage the versatile nature of 2-Deoxy-2-fluoro-D-galactose to craft biologically active molecules, pharmaceuticals, and functional materials. By strategically incorporating this compound into synthetic pathways, they can access a diverse array of structurally complex products with tailored properties and functions. In essence, 2-Deoxy-2-fluoro-D-galactose represents a valuable tool in the realm of chemical synthesis, enabling the creation of innovative compounds with potential applications across various industries.