16 Results for "

diketone

" in MedChemExpress (MCE) Product Catalog:
Products (16)

16 Results for "diketone" in MCE Product Catalog:

Art. -Nr.: HY-Y0779
CAS. Nr.: 403-42-9
Synonyms: 1-(4-Fluorophenyl)ethan-1-one
4'-Fluoroacetophenone (1-(4-Fluorophenyl)ethan-1-one) is p-fluoroacetophenone, and serves as a substrate for both SNAr dimerization reactions and cross SNAr reactions. 4'-Fluoroacetophenone is also an important intermediate that can be used in the synthesis of other active compounds, such as aromatic diketones .
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Art. -Nr.: HY-W000923
CAS. Nr.: 380430-49-9
(4-Boc-aminophenyl) boronic acid is an arylboronic acid. As a substrate in H2O, (4-Boc-aminophenyl) boronic acid participates in the CuO-catalyzed three-component reaction with α-ketoaldehydes and 1,3-dicarbonyl compounds to produce 1,4-diketone products .
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Art. -Nr.: HY-140448
CAS. Nr.: 2353409-85-3
Reinheit:  ≥95.0%
Target:  

PROTAC Linkers

Forschungsgebiete:  

Cancer

Diketone-PEG4-Biotin is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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Art. -Nr.: HY-130993
CAS. Nr.: 2097813-40-4
Isatropolone A, a natural product containing a 1,5-diketone moiety, is reisolated from Streptomyces Gö66. Isatropolone A shows potent activity against Leishmania donovani with an IC50 of 0.5 μM .
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Art. -Nr.: HY-140451
Target:  

PROTAC Linkers

Forschungsgebiete:  

Cancer

Diketone-PEG11-Diketone is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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Art. -Nr.: HY-W198670
CAS. Nr.: 704-00-7
Forschungsgebiete:  

Others

1,2-Diacetylbenzene, a γ-diketone metabolite derived from the neurotoxic solvent 1,2-diethylbenzene, is an aromatic hydrocarbon known for its reactivity with proteins.
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Art. -Nr.: HY-140450
Target:  

PROTAC Linkers

Forschungsgebiete:  

Cancer

Diketone-PEG12-DBCO is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs . Diketone-PEG12-DBCO is a click chemistry reagent, it contains a DBCO group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing Azide groups.
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Art. -Nr.: HY-140006
CAS. Nr.: 2353409-84-2
Target:  

PROTAC Linkers

Forschungsgebiete:  

Cancer

Diketone-PEG4-PFP ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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Art. -Nr.: HY-140447
Target:  

PROTAC Linkers

Forschungsgebiete:  

Cancer

Diketone-PEG11-PFP ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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Art. -Nr.: HY-140449
Target:  

PROTAC Linkers

Forschungsgebiete:  

Cancer

Diketone-PEG12-Biotin is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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Art. -Nr.: HY-120656
CAS. Nr.: 275816-51-8
Synonyms: PGK2
Forschungsgebiete:  

Metabolic Disease

Prostaglandin K2 (PGK2) is the 9,11-diketone formed by the oxidation of PGE2 or PGD2. Whether this compound exists biologically is uncertain; it is known to be resistant to metabolism by 15-hydroxy PGDH in vitro.
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Art. -Nr.: HY-W102669
CAS. Nr.: 82683-51-0
Target:  

Drug Intermediate

Forschungsgebiete:  

Cancer

Spiro[4.5]decane-7,9-dione (Compound 2e) is a cyclic 1,3-diketone. Spiro[4.5]decane-7,9-dione can be used in the study of glioma tumors .
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Art. -Nr.: HY-N11583
CAS. Nr.: 22054-39-3
Synonyms: Jasmololon
Jasmololone (compound 1c) is a reduced compound that can be oxidized by manganese dioxide to form the corresponding diketone .
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Art. -Nr.: HY-E71290
Forschungsgebiete:  

Others

β-Diketone hydrolase (EC 3.7.1.7) acts on the product of the action of EC 1.1.3.18 secondary-alcohol oxidase, on polyvinyl alcohols; involved in the bacterial degradation of polyvinyl alcohol.
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Art. -Nr.: HY-N19809
CAS. Nr.: 105377-71-7
10-Deacetyl-10-oxo-7-epi-taxol is a cytotoxic agent with a 9,10-diketone structure. 10-Deacetyl-10-oxo-7-epi-taxol induces cytotoxic activity in cancer cells .
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Art. -Nr.: HY-79587
CAS. Nr.: 134-81-6
Forschungsgebiete:  

Others

Benzil is a 1,2-diketone compound with multiple functions including photo-peroxidation initiator, crosslinking initiator and pattern-forming agent, and is commonly used as a precursor for photodegradable network crosslinkers. In oxygen-purged polymer films or glassy matrices, Benzil reacts with molecular oxygen under illumination at wavelengths greater than 370 nm or 400 nm, and converts to benzoyl peroxide in nearly quantitative yield. Subsequently, the generated benzoyl peroxide groups produce free radicals via thermal or photochemical decomposition, thereby enabling crosslinking of polymer chains, grafting of new monomers, and preparation of patterned polymers on solid surfaces using mask irradiation. Benzil also induces crosslinking of photodegradable poly (phenyl vinyl ketone) to form a stable photodegradable polymer network .
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