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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)-

Trichothec-9-en-8-one, 15-(acetyloxy)-12,13-epoxy-3,7-dihydroxy-,(3a,7a)-

CC(=O)OCC12C(C=C(C(=O)C1O)C)OC1C3(C2(C)CC1O)CO3 Request for Quotation
Chemical Name: Trichothec-9-en-8-one, 15-(acetyloxy)-12,13-epoxy-3,7-dihydroxy-,(3a,7a)-
CAS Number: 88337-96-6
Product Number: AG00GTGW(AGN-PC-0VKT0C)
Synonyms:
MDL No:
Molecular Formula: C17H22O7
Molecular Weight: 338.3524

Identification/Properties

Computed Properties
Molecular Weight:
338.356g/mol
XLogP3:
-0.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
3
Exact Mass:
338.137g/mol
Monoisotopic Mass:
338.137g/mol
Topological Polar Surface Area:
106A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
657
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
7
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


15-Acetoxy-3alpha,7alpha-dihydroxy-12,13-epoxytrichothec-9-en-8-one is a potent molecule widely applied in chemical synthesis due to its unique structural features and reactivity. This compound serves as a valuable building block for the synthesis of various complex organic compounds and natural products. In particular, its epoxide and hydroxyl functionalities make it a versatile intermediate in the synthesis of diverse bioactive molecules and pharmaceuticals. Additionally, the acetoxy group offers a site for further derivatization, allowing for the modification of its properties and enhancing its compatibility with specific synthetic pathways. With its rich chemistry and broad applicability, 15-Acetoxy-3alpha,7alpha-dihydroxy-12,13-epoxytrichothec-9-en-8-one plays a crucial role in the advancement of chemical synthesis strategies and the creation of new molecules with potential therapeutic applications.