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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)-

b-D-altro-2-Heptulopyranose, 2,7-anhydro-

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Chemical Name: b-D-altro-2-Heptulopyranose, 2,7-anhydro-
CAS Number: 469-90-9
Product Number: AG00DA7E(AGN-PC-0RUS1C)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Properties
MP:
101-102℃
Form:
Solid
Computed Properties
Molecular Weight:
192.167g/mol
XLogP3:
-2.5
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
192.063g/mol
Monoisotopic Mass:
192.063g/mol
Topological Polar Surface Area:
99.4A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
209
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


Sedoheptulosan, a rare sugar derivative with intriguing chemical properties, serves as a crucial building block in organic synthesis processes. Known for its unique seven-carbon backbone structure, Sedoheptulosan finds widespread application in the field of chemical synthesis due to its versatility and reactivity. In the realm of synthetic chemistry, Sedoheptulosan plays a vital role as a starting material for the creation of various organic compounds. It serves as a key intermediate in the synthesis of complex molecules, facilitating the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its ability to undergo selective functionalization reactions makes it a valuable tool for chemists seeking to construct intricate molecular structures with precision.Furthermore, Sedoheptulosan's distinctive structure allows for the synthesis of chemically diverse compounds that may not be easily accessible through conventional methods. This unique sugar derivative offers chemists a valuable platform for designing and developing novel chemical entities with desirable properties. Its incorporation into synthetic strategies enables the construction of structurally complex molecules with potential applications across a wide range of industries.Overall, Sedoheptulosan stands out as a versatile and indispensable component in the toolkit of synthetic chemists, providing a gateway to the synthesis of diverse organic compounds with tailored functionalities and applications. By harnessing the reactivity and structural features of Sedoheptulosan, chemists can unlock new possibilities in the realm of chemical synthesis, paving the way for innovative discoveries and advancements in the field.