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1,3,5-Trifluorobenzene CAS:372-38-3
1,3,5-Trifluorobenzene is a fluorinated aromatic compound characterized by three fluorine substituents positioned at the 1, 3, and 5 locations on a benzene ring. This compound is significant in organic chemistry due to the unique properties imparted by the fluorine atoms, including enhanced chemical stability and altered polarity. It serves as a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The presence of fluorine also influences molecular interactions, rendering 1,3,5-trifluorobenzene valuable in various research applications, particularly in areas focusing on drug discovery and materials science.
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2,4-Difluorobenzylamine CAS:72235-52-0
2,4-Difluorobenzylamine is an aromatic amine featuring two fluorine atoms positioned on the benzene ring at the 2 and 4 locations. This compound is notable for its unique chemical properties imparted by the fluorine substituents, which enhance both lipophilicity and reactivity. As a versatile building block in organic synthesis, 2,4-difluorobenzylamine plays a crucial role in the development of pharmaceuticals, agrochemicals, and advanced materials. Its ability to participate in various chemical reactions makes it valuable in medicinal chemistry, where it is explored for potential therapeutic applications.
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(S)-(+)-3-Chloro-1,2-propanediol CAS:60827-45-4
(S)-(+)-3-Chloro-1,2-propanediol is a chiral organic compound distinguished by its two hydroxyl (-OH) groups and a chlorine atom. This compound serves as an important intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. The specific stereochemistry of the (S)-(+)-enantiomer enhances its reactivity and biological properties, making it valuable for producing enantiomerically pure derivatives. Research continues to explore its diverse applications, ranging from drug development to functional materials, underscoring its relevance in both academic and industrial settings.
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(R)-(-)-3-Chloro-1,2-propanediol CAS:57090-45-6
(R)-(-)-3-Chloro-1,2-propanediol is a chiral organic compound that serves as an important intermediate in the synthesis of pharmaceuticals and agrochemicals. Its unique structure features two hydroxyl groups and a chlorine atom, making it a versatile building block for various chemical transformations. The specific stereochemistry of the (R)-(-)-enantiomer contributes to its reactivity and biological activity, allowing for the development of enantiomerically pure products. Ongoing research focuses on its applications in drug synthesis and as a potential precursor for other functionalized compounds, highlighting its significance in both medicinal chemistry and material science.
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(S)- (+)-Oxiran-2-ylmethyl- 3-nitrobenzenesulfonate CAS:115314-14-2
(S)-(+)-Oxiran-2-ylmethyl-3-nitrobenzenesulfonate is a chiral epoxide compound featuring an oxirane ring and a nitrobenzenesulfonate group. This compound has garnered interest in organic synthesis due to its unique reactivity, primarily attributed to the strained three-membered epoxide ring, which is highly susceptible to nucleophilic attack. The specific stereochemistry of the (S)-(+) enantiomer provides distinct advantages in asymmetric synthesis, enabling the production of enantiomerically pure compounds. Research continues to explore its applications in medicinal chemistry and materials science, highlighting its potential as a versatile intermediate for synthesizing pharmaceuticals and fine chemicals.
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(S)-(+)-Epichlorohydrin CAS:67843-74-7
(S)-(+)-Epichlorohydrin is a chiral organic compound and an important building block in organic synthesis, known for its versatile applications in the production of epoxy resins, pharmaceuticals, and agrochemicals. Characterized by its three-membered epoxide ring and a chlorine atom, this compound exhibits significant reactivity due to its electrophilic nature. The enantiomerically pure form, (S)-(+)-epichlorohydrin, is of particular interest in asymmetric synthesis, allowing for the development of enantiomerically enriched products. Research continues to explore its utility and mechanisms, contributing to advancements in both industrial processes and medicinal chemistry.
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2,4,5-Trifluorobenzyl alcohol CAS:144284-25-3
2,4,5-Trifluorobenzyl alcohol is a fluorinated aromatic compound with significant applications in pharmaceuticals and agrochemicals. The presence of three fluorine atoms at the 2, 4, and 5 positions on the benzene ring enhances the compound’s chemical stability and lipophilicity, making it an important building block in organic synthesis. Its unique properties allow for modifications that can lead to the development of new therapeutic agents. As research into fluorinated compounds continues to grow, 2,4,5-trifluorobenzyl alcohol is being explored for its potential in drug discovery and material science, highlighting its relevance in modern chemistry.
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(S)-(-)-4-Chloromethyl-2,2-dimethyl-1,3-dioxolane CAS:60456-22-6
(S)-(-)-4-Chloromethyl-2,2-dimethyl-1,3-dioxolane is a chiral compound with a unique dioxolane structure that features both a chloromethyl group and two methyl substituents. This compound has garnered attention in the field of organic synthesis for its potential use as an intermediate in the preparation of various pharmaceuticals and fine chemicals. The specific stereochemistry of the (S)-(-) enantiomer can significantly influence its reactivity and selectivity in chemical reactions, making it valuable for asymmetric synthesis. Ongoing research aims to explore its applications and reactions, highlighting its significance in material science and medicinal chemistry.
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2,5-Dibromopyrimidine CAS:32779-37-6
2,5-Dibromopyrimidine is a halogenated pyrimidine derivative with significant implications in organic synthesis and pharmaceutical chemistry. This compound features two bromine atoms attached to the 2 and 5 positions of the pyrimidine ring, enhancing its reactivity and versatility. Its molecular formula is C4H2Br2N2, and it serves as an important building block in the synthesis of various bioactive compounds, including pharmaceuticals and agrochemicals. The presence of bromine enhances electrophilic aromatic substitution reactions, making 2,5-dibromopyrimidine a valuable intermediate for constructing complex molecules in medicinal chemistry and materials science.
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(R)-(-)-Glycidyl butyrate CAS:60456-26-0
(R)-(-)-Glycidyl butyrate is a chiral epoxy compound characterized by the presence of both an epoxide group and a butyrate ester. It serves as an important intermediate in organic synthesis, particularly in the development of pharmaceuticals, agrochemicals, and specialty polymers. The unique structure of this compound allows for versatile chemical transformations, making it valuable in various applications. The specific stereochemistry of the (R)-(-) enantiomer can influence its reactivity and biological interactions, highlighting its significance in asymmetric synthesis and material science. Research continues to explore its potential uses and modifications in diverse fields.
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DL-4-HYDROXYPHENYLGLYCINE CAS:938-97-6
DL-4-Hydroxyphenylglycine is a chiral amino acid derivative characterized by the presence of a hydroxyl group on the phenyl ring attached to the glycine backbone. With the molecular formula C9H11NO3, it exists as a racemic mixture of its D- and L-enantiomers. This compound has attracted interest in pharmaceutical and medicinal chemistry due to its potential biological activities, particularly in modulating neurotransmitter systems. As a versatile building block, DL-4-hydroxyphenylglycine is utilized in the synthesis of various bioactive compounds, offering insights into therapeutic applications for conditions such as pain management and neurodegenerative disorders.
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D-2-Phenylglycine CAS:875-74-1
D-2-Phenylglycine is a chiral amino acid with the molecular formula C8H9NO2. It features a phenyl group attached to the second carbon of the glycine backbone, which imparts unique properties and biological activities. This compound exists as one of the enantiomers of 2-phenylglycine, specifically the D-form, and has garnered significant attention in pharmaceutical chemistry due to its potential applications in drug development. D-2-Phenylglycine serves as an important building block for synthesizing various biologically active molecules and is investigated for its potential roles in neuromodulation, analgesia, and anti-inflammatory therapies.
