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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)-

D-Fructose, 1-chloro-1-deoxy-

OC[C@H]([C@H]([C@@H](C(=O)CCl)O)O)O Request for Quotation
Chemical Name: D-Fructose, 1-chloro-1-deoxy-
CAS Number: 32785-93-6
Product Number: AG00CI1U(AGN-PC-0O8Y5T)
Synonyms:
MDL No:
Molecular Formula: C6H11ClO5
Molecular Weight: 198.60154

Identification/Properties

Computed Properties
Molecular Weight:
198.6g/mol
XLogP3:
-1.6
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
198.029501g/mol
Monoisotopic Mass:
198.029501g/mol
Topological Polar Surface Area:
90.2Ų
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
166
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Chloro-1-deoxy-d-fructose, also known as chloro-d-fructose, is a key compound used in chemical synthesis for its unique reactivity and versatility. This compound serves as an important building block in the preparation of various carbohydrate derivatives and complex organic molecules. In particular, 1-chloro-1-deoxy-d-fructose is often employed in the synthesis of carbohydrate-based pharmaceuticals, agrochemicals, and specialty chemicals. Its ability to undergo selective reactions with nucleophiles makes it a valuable tool for chemists looking to introduce specific functional groups into their target molecules. Additionally, the presence of the chloro group on the fructose scaffold allows for further derivatization through substitution or elimination reactions, enabling the creation of diverse chemical libraries for drug discovery and material science applications.