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Dihydrofurans

Organic heterocyclic compounds that consist of a five-membered ring with one oxygen atom and four carbon atoms; they are considered enol ethers.
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Search Within Results
Keyword Search:
46 – 60 of 73 results
46

Aobchem N -(dihydrofuran-3(2H)-ylidene)-4-methylbenzenesulfonohydrazide | 97% | CAS 1708-19-6 | C11H14N2O3S | 25g

N -(dihydrofuran-3(2H)-ylidene)-4-methylbenzenesulfonohydrazide | 97% | CAS 1708-19-6 | C11H14N2O3S | 25g

ENCOMPASS_PREFERRED
47

Ambeed AMBEED

5000869622 25-DIHYDROFURAN-3-CARBOX 100MG

ENCOMPASS_PREFERRED
48

Aobchem N -(dihydrofuran-3(2H)-ylidene)-4-methylbenzenesulfonohydrazide | 97% | CAS 1708-19-6 | C11H14N2O3S | 500mg

N -(dihydrofuran-3(2H)-ylidene)-4-methylbenzenesulfonohydrazide | 97% | CAS 1708-19-6 | C11H14N2O3S | 500mg

ENCOMPASS_PREFERRED
49

Aobchem N -(dihydrofuran-3(2H)-ylidene)-4-methylbenzenesulfonohydrazide | 97% | CAS 1708-19-6 | C11H14N2O3S | 5g

N -(dihydrofuran-3(2H)-ylidene)-4-methylbenzenesulfonohydrazide | 97% | CAS 1708-19-6 | C11H14N2O3S | 5g

ENCOMPASS_PREFERRED
50

Aobchem Stannane (2 6-difluorophenyl)trimethyl- | 95% | CAS 55204-79-0 | C9H12F2Sn | 5g

Stannane (2 6-difluorophenyl)trimethyl- | 95% | CAS 55204-79-0 | C9H12F2Sn | 5g

ENCOMPASS_PREFERRED
51

Aobchem N -(dihydrofuran-3(2H)-ylidene)-4-methylbenzenesulfonohydrazide | 97% | CAS 1708-19-6 | C11H14N2O3S | 250mg

N -(dihydrofuran-3(2H)-ylidene)-4-methylbenzenesulfonohydrazide | 97% | CAS 1708-19-6 | C11H14N2O3S | 250mg

ENCOMPASS_PREFERRED
52

eMolecules​ 541-57-1 | 4-Hydroxy-2,5-dihydrofuran-2-one | Combi-Blocks | MFCD00052187 | 100.073 | C4H4O3 | 97.000 | OC1=CC(=O)OC1 | 1g | 401043050

4-Hydroxy-2,5-dihydrofuran-2-one | Combi-Blocks | 541-57-1 | MFCD00052187 | 100.073 | C4H4O3 | 97.000 | OC1=CC(=O)OC1 | 1g | 401043050

ENCOMPASS_PREFERRED
53

Chemscene ChemScene | 2-(4,5-Dihydrofuran-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | 100MG | CS-0100813 | 0.97 | 1046812-03-6| MFCD13182120 | 196.05

ChemScene | 2-(4,5-Dihydrofuran-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | 100MG | CS-0100813 | 0.97 | 1046812-03-6| MFCD13182120 | 196.05

ENCOMPASS_PREFERRED
54

Sigma Aldrich Fine Chemicals Biosciences Aflatoxin B1 from Aspergillus flavus from Aspergillus flavus | 1162-65-8 | MFCD00869647 | 50MG

Aflatoxin B1 from Aspergillus flavus from Aspergillus flavus | Purity: >=98.0% (HPLC) | Mol Wt: 312.27 | 1162-65-8 | MFCD00869647 | 50MG

ENCOMPASS
55

Sigma Aldrich Fine Chemicals Biosciences Aflatoxin B1 from Aspergillus Flavus | 1162-65-8 | MFCD00869647 | 5mg

Aflatoxin B1 from Aspergillus Flavus | Purity: 98% | Mol Wt: 312.27 | 1162-65-8 | MFCD00869647 | 5mg

ENCOMPASS
56

Ambeed 2 6Dimethoxy4hydroxybenzaldehy

2,6-Dimethoxy-4-hydroxybenzaldehyde, 22080-96-2, 98%

ENCOMPASS_PREFERRED
57

eMolecules​ 108-30-5 | Succinic anhydride | Ambeed | MFCD00005525 | 100.073 | C4H4O3 | 97.000 | O=C1CCC(=O)O1 | 25g | 587278512

Succinic anhydride | Ambeed | 108-30-5 | MFCD00005525 | 100.073 | C4H4O3 | 97.000 | O=C1CCC(=O)O1 | 25g | 587278512

ENCOMPASS_PREFERRED
58

eMolecules​ 22929-52-8 | Dihydrofuran-3(2H)-one | ChemScene | MFCD07778393 | 86.090 | C4H6O2 | 98.000 | O=C1CCOC1 | 10g | 346744963

Dihydrofuran-3(2H)-one | ChemScene | 22929-52-8 | MFCD07778393 | 86.090 | C4H6O2 | 98.000 | O=C1CCOC1 | 10g | 346744963

ENCOMPASS_PREFERRED
59

eMolecules​ 22929-52-8 | Dihydrofuran-3(2H)-one | Apollo Scientific | MFCD07778393 | 86.090 | C4H6O2 | 95.000 | O=C1CCOC1 | 10g | 686663413

Dihydrofuran-3(2H)-one | Apollo Scientific | 22929-52-8 | MFCD07778393 | 86.090 | C4H6O2 | 95.000 | O=C1CCOC1 | 10g | 686663413

ENCOMPASS_PREFERRED
60

Apexbio Technology LLC DIHYDROFURAN-32H-ONE-500MG

Dihydrofuran-3(2H)-one (CAS No 22929-52-8) is a compound of interest in the field of organic chemistry and pharmaceutical research Originating from furan derivatives it is studied for its potential role in modulating biochemical pathways involving lactone rings which are significant in various metabolic processes Its mechanism of action often involves targeting enzyme-catalyzed reactions showcasing inhibitory activity in certain pathways In vitro its activity is generally observed in the nanomolar to low micromolar range This compound is commonly utilized in drug discovery and screening serving as a scaffold for developing therapeutic agents Typical applications include use in cell models and animal studies to investigate pharmacodynamic and pharmacokinetic profiles Experimental concentrations typically depend on the specific research design ensuring optimal engagement with the intended biochemical targets and achieving desired outcomes

ENCOMPASS_PREFERRED