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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)-

4-[tert-butyl(dimethyl)silyl]oxyoxane-2,6-dione

CC([Si](OC1CC(=O)OC(=O)C1)(C)C)(C)C Request for Quotation
Chemical Name: 4-[tert-butyl(dimethyl)silyl]oxyoxane-2,6-dione
CAS Number: 91424-40-7
Product Number: AG003IAB(AGN-PC-0L61SH)
Synonyms:
MDL No: MFCD00075235
Molecular Formula: C11H20O4Si
Molecular Weight: 244.3596

Identification/Properties

Properties
MP:
79-81 °C(lit.)
BP:
302.4 °C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Stability:
Moisture Sensitive
Refractive Index:
1.4510
Computed Properties
Molecular Weight:
244.362g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
244.113g/mol
Monoisotopic Mass:
244.113g/mol
Topological Polar Surface Area:
52.6A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
288
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]dihydro-2H-pyran-2,6(3H)-dione is a versatile compound widely used in chemical synthesis as a protecting group for alcohols. This compound plays a crucial role in organic synthesis by temporarily masking the hydroxyl group of alcohols, thus allowing for selective reactions to occur at other functional groups within a molecule. By utilizing this protecting group strategy, chemists can control the reactivity of specific functional groups and guide the synthesis towards the desired product. This compound's stability and ease of removal make it a valuable tool in the synthesis of complex organic molecules where precise manipulation of functional groups is necessary.