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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)-

threo-Pent-1-enitol, 1,5-anhydro-2-deoxy-, diacetate

CC(=O)O[C@@H]1C=COC[C@H]1OC(=O)C Request for Quotation
Chemical Name: threo-Pent-1-enitol, 1,5-anhydro-2-deoxy-, diacetate
CAS Number: 3152-43-0
Product Number: AG00CI1N(AGN-PC-0O8UDV)
Synonyms:
MDL No:
Molecular Formula: C9H12O5
Molecular Weight: 200.18858

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
200.19g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
200.068g/mol
Monoisotopic Mass:
200.068g/mol
Topological Polar Surface Area:
61.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
258
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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


The 1,1'-((3R,4R)-3,4-Dihydro-2H-pyran-3,4-diyl)diethanone is a highly versatile compound widely utilized in chemical synthesis. Its unique structural properties make it an indispensable building block in the creation of various advanced organic molecules. In chemical synthesis, this compound serves as a key intermediate in the formation of complex structures due to its ability to undergo diverse chemical reactions with different functional groups. Specifically, it is commonly employed in the construction of elaborate natural products and pharmaceutical compounds where its presence can contribute significantly to the overall molecular architecture and function. Additionally, its stereochemistry plays a crucial role in dictating the outcome of synthetic routes, making it a valuable tool for chemists seeking to control the stereochemical outcomes of their reactions. Overall, the application of 1,1'-((3R,4R)-3,4-Dihydro-2H-pyran-3,4-diyl)diethanone in chemical synthesis showcases its importance in the development of innovative and complex organic compounds.