Synthesis Reagents
Items 51 to 55 of 55 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Mesoporphyrin IX dihydrochloride | 68938-72-7 | sc-235601 | 50 mg | $127.00 | 1 | |
Mesoporphyrin IX dihydrochloride serves as a versatile synthesis reagent, notable for its ability to coordinate with metal ions, forming stable complexes that can influence reaction pathways. Its unique porphyrin structure allows for effective light absorption, which can be harnessed in photochemical reactions. Additionally, its solubility in various solvents enhances its reactivity, making it a key player in catalyzing transformations and facilitating intricate molecular assemblies. | ||||||
6-chlorochromane-3-carboxylic acid | 164265-01-4 | sc-278501 | 250 mg | $125.00 | ||
6-Chlorochromane-3-carboxylic acid is a distinctive synthesis reagent characterized by its ability to engage in electrophilic aromatic substitution reactions due to the presence of the chlorinated chromane moiety. Its carboxylic acid functional group enhances reactivity through hydrogen bonding, promoting interactions with nucleophiles. This compound's unique steric and electronic properties facilitate selective transformations, making it a valuable tool in complex organic synthesis pathways. | ||||||
5-(3-Iodopropoxy)-2-nitrobenzyl alcohol | 185994-27-8 | sc-317521 sc-317521A | 250 mg 1 g | $150.00 $412.00 | ||
5-(3-Iodopropoxy)-2-nitrobenzyl alcohol serves as a versatile synthesis reagent, notable for its ability to participate in nucleophilic substitution reactions. The presence of the nitro group enhances electrophilicity, allowing for efficient coupling with various nucleophiles. Its unique propoxy chain introduces steric hindrance, influencing reaction selectivity and kinetics. This compound's distinctive molecular interactions enable tailored transformations in synthetic organic chemistry. | ||||||
4-Isoquinolineboronic acid | 192182-56-2 | sc-254690 sc-254690A sc-254690B | 1 g 5 g 10 g | $40.00 $115.00 $225.00 | ||
4-Isoquinolineboronic acid is a specialized synthesis reagent recognized for its ability to facilitate cross-coupling reactions, particularly in the formation of carbon-carbon bonds. The boronic acid moiety exhibits strong coordination with transition metals, enhancing catalytic efficiency. Its isoquinoline structure contributes to unique π-π stacking interactions, which can influence reaction pathways and selectivity. This compound's reactivity profile allows for diverse applications in complex organic synthesis. | ||||||
α-Methyl-4-(methylsulfonyl)benzylamine | 387350-90-5 | sc-285851 | 1 g | $200.00 | ||
α-Methyl-4-(methylsulfonyl)benzylamine serves as a versatile synthesis reagent, notable for its ability to engage in nucleophilic substitution reactions. The presence of the methylsulfonyl group enhances its electrophilic character, promoting efficient interactions with electrophiles. Its unique steric and electronic properties facilitate selective pathways in multi-step syntheses, while the amine functionality allows for hydrogen bonding, influencing reaction kinetics and product formation. | ||||||