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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)-

1,4-Benzenediol, 2-methyl-, diacetate

Oc1ccc(c(c1)C)O.CC(=O)O.CC(=O)O Request for Quotation
Chemical Name: 1,4-Benzenediol, 2-methyl-, diacetate
CAS Number: 717-27-1
Product Number: AG003FWI(AGN-PC-0OH0S4)
Synonyms:
MDL No:
Molecular Formula: C11H16O6
Molecular Weight: 244.24114

Identification/Properties

Properties
MP:
41-45℃(lit.)
Storage:
Room Temperature;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
208.213g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
208.074g/mol
Monoisotopic Mass:
208.074g/mol
Topological Polar Surface Area:
52.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
249
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#:
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


2,5-Diacetoxytoluene is a versatile compound widely used in chemical synthesis as a key building block for various organic reactions. This compound is commonly employed in the production of pharmaceuticals, agrochemicals, and fragrances due to its unique reactivity and functional groups. Its acetoxy groups can undergo a range of transformations, such as deacetylation, acylation, and reduction, making it valuable for creating a diverse array of organic molecules. In particular, 2,5-Diacetoxytoluene is frequently used in the synthesis of complex heterocyclic compounds, which are essential in drug discovery and development. Its ability to participate in multiple types of reactions makes it an indispensable tool for chemists seeking to construct intricate organic structures with high efficiency and precision.