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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-D-Glucofuranuronic acid, 1,2-O-(1-methylethylidene)-, g-lactone

O[C@@H]1C(=O)O[C@H]2[C@@H]1O[C@H]1[C@@H]2OC(O1)(C)C Request for Quotation
Chemical Name: a-D-Glucofuranuronic acid, 1,2-O-(1-methylethylidene)-, g-lactone
CAS Number: 20513-98-8
Product Number: AG0029WD(AGN-PC-0QV1JS)
Synonyms:
MDL No:
Molecular Formula: C9H12O6
Molecular Weight: 216.1880

Identification/Properties

Computed Properties
Molecular Weight:
216.189g/mol
XLogP3:
-0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
0
Exact Mass:
216.063g/mol
Monoisotopic Mass:
216.063g/mol
Topological Polar Surface Area:
74.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
314
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,2-O-Isopropylidene-α-D-glucurono-6,3-lactone, also known as $name$, serves as a valuable chemical building block in organic synthesis. This compound is commonly utilized in chemical reactions as a protecting group for the hydroxyl functionality. By selectively blocking specific hydroxyl groups within a molecule with $name$, chemists are able to protect these groups from unwanted reactions or modifications during various synthetic procedures. This protective group can subsequently be removed under specific conditions to reveal the original hydroxyl groups, enabling further functionalization and manipulation of the molecule. Overall, the application of 1,2-O-Isopropylidene-α-D-glucurono-6,3-lactone in chemical synthesis plays a crucial role in controlling the reactivity and selectivity of hydroxyl-containing compounds, allowing for the efficient and precise construction of complex organic molecules.