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4-Hydroxyphenylacetone CAS:770-39-8
4-Hydroxyphenylacetone is an aromatic ketone that features a hydroxyl group attached to the phenyl ring and an acetone moiety. This compound is recognized for its diverse applications in organic synthesis and medicinal chemistry. It serves as an important intermediate in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. The presence of the hydroxy group enhances its reactivity and allows for further modifications, making it a valuable scaffold for drug development. Research into 4-hydroxyphenylacetone has highlighted its potential biological activities, including antioxidant and anti-inflammatory properties, which contribute to its relevance in pharmacological studies.
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3-(4-Chlorbutyl)-1H-indol-5-carbonitril CAS:143612-79-7
3-(4-Chlorobutyl)-1H-indol-5-carbonitrile is an indole derivative characterized by a unique combination of indole and nitrile functional groups, along with a chlorobutyl side chain. This compound has gained attention in the field of medicinal chemistry due to its potential biological activities, which may include antimicrobial, anti-inflammatory, and anticancer properties. The indole scaffold serves as a versatile backbone for designing pharmaceuticals, while the presence of the chlorobutyl group enhances its lipophilicity, potentially improving bioavailability. Ongoing research aims to explore the therapeutic applications and mechanisms of action associated with this compound.
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Amlodipine Base CAS:88150-42-9
Amlodipine Base is a potent calcium channel blocker primarily utilized in the management of hypertension and angina pectoris. Its pharmacological action involves inhibiting calcium ion influx into vascular smooth muscle and cardiac tissue, leading to vasodilation and reduced myocardial oxygen demand. Amlodipine’s long half-life allows for convenient once-daily dosing, enhancing patient adherence to treatment regimens. As a member of the dihydropyridine class, it is well-tolerated, with a favorable safety profile. The compound has become a staple medication in cardiovascular therapy due to its effectiveness in improving clinical outcomes for patients with various cardiovascular conditions.
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2-Methoxyphenylacetone CAS:5211-62-1
2-Methoxyphenylacetone is an aromatic ketone distinguished by a methoxy group attached to the phenyl ring and an acetone functional group. This compound has garnered attention for its utility in organic synthesis and as a potential bioactive molecule in medicinal chemistry. The presence of the methoxy substituent enhances its solubility and reactivity, making it a versatile building block for the development of more complex structures. Research has begun to explore the biological activities associated with 2-methoxyphenylacetone, suggesting potential applications in pharmaceuticals, particularly in the fields of anti-inflammatory and analgesic agents.
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1-Methylindazole-3-carboxylic acid CAS:50890-83-0
1-Methylindazole-3-carboxylic acid is a heterocyclic organic compound known for its biologically active properties and diverse applications in medicinal chemistry. This compound features an indazole framework with a methyl group and a carboxylic acid functional group, which contribute to its chemical reactivity and potential therapeutic effects. It has garnered interest for its role as a building block in the synthesis of various pharmaceuticals and agrochemicals. The unique structural characteristics of 1-methylindazole-3-carboxylic acid enable it to participate in a range of chemical reactions, making it a valuable target for researchers exploring new drug candidates.
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2-Bromophenylacetone CAS:21906-31-0
2-Bromophenylacetone is an aromatic ketone featuring a bromine substituent in the meta position of the phenyl ring, coupled with an acetone functional group. This compound has gained significant interest in organic synthesis and medicinal chemistry due to its utility as a versatile building block for the development of more complex molecules, including various pharmaceuticals. The presence of the bromine atom enhances electrophilic reactivity, facilitating further chemical transformations. Additionally, 2-bromophenylacetone may exhibit notable biological activities, making it a subject of research for potential therapeutic applications in areas such as antimicrobial and anti-inflammatory agents.
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BOC-SER(ME)-OH CAS:51293-47-1
BOC-SER(ME)-OH, or tert-butyloxycarbonyl-serine methyl ester, is a protected amino acid derivative commonly used in peptide synthesis and medicinal chemistry. The BOC (tert-butyloxycarbonyl) group serves as a protective moiety, facilitating the selective reaction of the amino group during peptide formation, while the serine residue contributes to the structural and functional diversity of peptides and proteins. This compound’s unique structure makes it a vital building block in the development of bioactive peptides and pharmaceuticals, particularly those targeting various biological pathways. Its application in solid-phase peptide synthesis further underscores its importance in contemporary organic chemistry.
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5-Bromo-7-azaindole CAS:183208-35-7
5-Bromo-7-azaindole is a nitrogen-containing heterocyclic compound that belongs to the indole family, specifically characterized by the incorporation of a bromine atom and a nitrogen atom in its ring structure. This compound has gained interest in medicinal chemistry due to its potential biological activities, including antitumor and antimicrobial properties. The 7-aza substitution allows for unique interactions with biological targets, potentially influencing enzyme inhibition and receptor binding. As researchers continue to explore its applications, 5-bromo-7-azaindole represents a promising scaffold for the development of novel pharmaceuticals aimed at treating various diseases.
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5-Acetonyl-2-methoxybenzene sulfonamide CAS:116091-63-5
5-Acetonyl-2-methoxybenzene sulfonamide is an organic compound notable for its sulfonamide functionality and unique aromatic structure. This compound comprises a methoxy group, an acetonyl substituent, and a sulfonamide moiety, which contributes to its diverse chemical properties and potential biological activities. Sulfonamides have been traditionally recognized for their antimicrobial properties, while the specific structural features of 5-acetonyl-2-methoxybenzene sulfonamide may enhance its reactivity and pharmacological profile. As researchers explore its synthesis and applications, this compound has emerged as a promising candidate in medicinal chemistry, particularly for developing innovative therapeutic agents.
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2-Amino-2-ethyl-1,3-propanediol CAS:115-70-8
2-Amino-2-ethyl-1,3-propanediol, often referred to as AEPD, is a branched-chain amino alcohol characterized by the presence of both amino and hydroxyl functional groups. This compound possesses a unique structure that enhances its solubility and reactivity in various chemical environments. It is known for its role as a buffering agent and an important building block in organic synthesis. Due to these properties, AEPD has garnered attention in pharmaceutical development, biochemical research, and cosmetic formulations.
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1-TERT-BUTOXY-2-PROPANOL CAS:57018-52-7
1-Tert-butoxy-2-propanol is a tertiary alcohol characterized by the presence of a tert-butoxy group and a propanol backbone. This compound exhibits properties typical of alcohols, such as good solubility in organic solvents and moderate polarity. Its unique structure provides it with specific reactivity, making it useful as a solvent and a reagent in various chemical processes. Researchers and industries value this compound for its versatility in applications across organic synthesis and formulation chemistry.
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Bis(neopentyl glycolato)diboron CAS:201733-56-4
Bis(neopentyl glycolato)diboron is an organoboron compound characterized by two neopentyl glycolate ligands coordinated to a central diboron unit. This compound is valued for its unique chemical properties, including its ability to act as a reagent in various chemical reactions. Its structure allows it to participate in boron-mediated transformations, making it a significant intermediate in synthetic organic chemistry. Due to the presence of the glycolate moiety, this compound is also known for its solubility in polar solvents and compatibility with diverse functional groups, contributing to its utility in various applications.
