Date published: 2025-10-19

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Furans

Santa Cruz Biotechnology now offers a broad range of furans for use in various applications. Furans, a class of heterocyclic organic compounds characterized by a five-membered aromatic ring with four carbon atoms and one oxygen atom, are essential in scientific research due to their unique chemical properties and versatility. These compounds are pivotal in organic synthesis, where they serve as intermediates in the production of a wide array of chemicals, including agrochemicals, and polymers. Researchers in synthetic chemistry utilize furans to develop novel synthetic routes and to create complex molecular architectures with potential applications in material science and industrial processes. In environmental science, furans are studied for their presence and formation during the combustion of organic materials, making them important markers in pollution studies and environmental monitoring. Analytical chemists employ techniques such as gas chromatography-mass spectrometry (GC-MS) to detect and quantify furans in various matrices, aiding in the investigation of their distribution and environmental impact. Furthermore, furans are significant in the field of renewable energy, where they are explored as building blocks for the synthesis of biofuels and bioplastics, contributing to the development of sustainable and eco-friendly alternatives to traditional fossil fuel-based products. By offering a diverse selection of furans, Santa Cruz Biotechnology supports a wide range of scientific endeavors, enabling researchers to select the appropriate furan for their specific experimental needs. This extensive range of furans facilitates innovation and discovery across multiple scientific disciplines, including organic chemistry, environmental science, analytical chemistry, and renewable energy research. View detailed information on our available furans by clicking on the product name.

Items 31 to 40 of 98 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Ranitidine

66357-35-5sc-203679
1 g
$189.00
(1)

Ranitidine, as a furan derivative, exhibits intriguing properties due to its unique electronic structure, which allows for selective interactions with electrophiles. The furan ring's aromaticity contributes to its stability while enabling participation in electrophilic aromatic substitution reactions. Its ability to form hydrogen bonds enhances solubility in polar solvents, influencing reaction kinetics. Furthermore, the compound's steric configuration can affect its reactivity, leading to diverse synthetic pathways.

Darunavir

206361-99-1sc-218079
5 mg
$311.00
4
(1)

Darunavir, classified as a furan, showcases distinctive reactivity patterns attributed to its electron-rich furan ring, which facilitates nucleophilic attack in various chemical transformations. The compound's planar structure enhances π-π stacking interactions, influencing its aggregation behavior in solution. Additionally, the presence of functional groups allows for versatile coordination with metal catalysts, potentially altering reaction mechanisms and enhancing selectivity in synthetic applications.

NSC697923

343351-67-7sc-391107
sc-391107A
1 mg
5 mg
$15.00
$51.00
3
(1)

NSC697923, a furan derivative, exhibits intriguing electronic properties due to its conjugated system, which promotes unique charge transfer interactions. Its structural rigidity contributes to enhanced stability under various conditions, while the presence of substituents can modulate its reactivity. The compound's ability to engage in cycloaddition reactions highlights its potential for forming complex molecular architectures, making it a subject of interest in synthetic chemistry.

PPQ-102

931706-15-9sc-364673
10 mg
$298.00
1
(1)

PPQ-102, a furan derivative, showcases remarkable reactivity as an acid halide, facilitating nucleophilic acyl substitution with high efficiency. Its electron-rich furan ring enhances electrophilicity, allowing for rapid interactions with various nucleophiles. The compound's unique steric and electronic properties enable selective pathways in polymerization reactions, while its ability to form stable intermediates contributes to its versatility in synthetic applications.

YC-1

170632-47-0sc-202856
sc-202856A
sc-202856B
sc-202856C
1 mg
5 mg
10 mg
50 mg
$32.00
$122.00
$214.00
$928.00
9
(1)

YC-1, a furan compound, exhibits intriguing reactivity patterns as an acid halide, characterized by its ability to engage in rapid electrophilic reactions. The presence of the furan moiety enhances its susceptibility to nucleophilic attack, leading to diverse reaction pathways. Its distinct electronic structure promotes unique intermolecular interactions, influencing reaction kinetics and enabling the formation of complex adducts. This behavior underscores its potential in various synthetic transformations.

Kahweol

6894-43-5sc-203089B
sc-203089
sc-203089A
5 mg
10 mg
25 mg
$88.00
$153.00
$357.00
9
(1)

Kahweol, a furan derivative, showcases remarkable reactivity as an acid halide, primarily due to its electron-rich furan ring. This structure facilitates unique resonance stabilization, allowing for selective electrophilic substitutions. Its ability to form stable intermediates enhances reaction rates, while the steric properties of its substituents influence the regioselectivity of nucleophilic attacks. These characteristics contribute to its versatility in synthetic organic chemistry.

PYR 41

418805-02-4sc-362786
sc-362786A
5 mg
25 mg
$72.00
$153.00
1
(1)

PYR 41, a furan-based compound, exhibits intriguing reactivity patterns as an acid halide, driven by its conjugated π-electron system. This configuration promotes strong dipole interactions, enhancing its electrophilic character. The compound's unique steric environment allows for diverse reaction pathways, leading to varied product distributions. Additionally, its solubility in polar solvents influences reaction kinetics, making it a notable candidate for exploring novel synthetic routes.

DAR-4M AM

sc-221530
1 mg
$1199.00
3
(1)

DAR-4M AM, a furan derivative, showcases remarkable reactivity as an acid halide, characterized by its electron-rich furan ring that facilitates nucleophilic attack. The compound's planar structure and resonance stabilization contribute to its selective reactivity, allowing for efficient formation of acylation products. Its ability to engage in rapid intermolecular interactions enhances reaction rates, while its compatibility with various solvents opens avenues for innovative synthetic methodologies.

Cafestol

469-83-0sc-204663
50 mg
$260.00
4
(1)

Cafestol, a furan compound, exhibits intriguing properties as an acid halide, primarily due to its unique electronic configuration. The presence of multiple functional groups allows for diverse reaction pathways, promoting selective acylation reactions. Its steric hindrance influences reaction kinetics, leading to distinct product distributions. Additionally, Cafestol's solubility in organic solvents enhances its versatility in synthetic applications, making it a valuable intermediate in organic chemistry.

(+)-O,O′-Diacetyl-L-tartaric anhydride

6283-74-5sc-250604
25 g
$97.00
(1)

(+)-O,O'-Diacetyl-L-tartaric anhydride, a furan derivative, showcases remarkable reactivity as an acid halide, characterized by its ability to form stable intermediates through intramolecular interactions. The compound's unique stereochemistry facilitates regioselective acylation, while its anhydride functionality promotes rapid esterification reactions. Its polar nature enhances solvation dynamics, influencing reaction rates and product formation in various organic transformations.