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  • 2-Chloro-4-(trifluoromethyl)pyridine  CAS:81565-18-6

    2-Chloro-4-(trifluoromethyl)pyridine CAS:81565-18-6

    2-Chloro-4-(trifluoromethyl)pyridine is a pyridine derivative with the molecular formula C6H3ClF3N. It features a chlorine atom at the 2-position and a trifluoromethyl group (-CF3) at the 4-position of the pyridine ring. This compound is of significant interest in organic synthesis and is notable for its unique electronic properties and lipophilicity, which are influenced by the presence of the electronegative trifluoromethyl group. Its structure makes it useful as a versatile building block in the development of various chemical products.

     

  • 2,6-Difluoro-3-iodopyridine CAS:685517-67-3

    2,6-Difluoro-3-iodopyridine CAS:685517-67-3

    2,6-Difluoro-3-iodopyridine is a halogenated pyridine derivative with the molecular formula C5H3F2IN. It features iodine at the 3-position and fluorine substituents at the 2 and 6-positions of the pyridine ring. This compound is of interest in synthetic organic chemistry due to its unique electronic properties and reactivity, which are influenced by the presence of both electronegative fluorine and iodine atoms. It serves as a versatile building block for generating diverse chemical compounds in various fields, including pharmaceuticals and agrochemicals.

  • 4-Bromo-2,6-difluorobenzaldehyde CAS:537013-51-7

    4-Bromo-2,6-difluorobenzaldehyde CAS:537013-51-7

    4-Bromo-2,6-difluorobenzaldehyde is an aromatic compound with the molecular formula C7H4BrF2O. It features a benzene ring substituted with a bromine atom at the 4-position and two fluorine atoms at the 2 and 6-positions, along with an aldehyde functional group (-CHO). This unique structure imparts distinct electronic properties, making it a valuable intermediate in organic synthesis and pharmaceutical applications. Its reactivity and stability are influenced by the presence of both electronegative fluorine and bromine substituents.

  • 4-Iodobenzenesulfonyl chloride CAS:98-61-3

    4-Iodobenzenesulfonyl chloride CAS:98-61-3

    4-Iodobenzenesulfonyl chloride, often abbreviated as IBSC, is an aromatic sulfonyl chloride compound with the chemical formula C7H6ClIO2S. It features a sulfonyl group (-SO2) attached to a benzene ring that also has an iodine substituent at the para position. This compound is typically utilized in organic synthesis due to its effective electrophilic characteristics, making it a valuable reagent in various chemical reactions. Its reactive nature allows it to participate in sulfonylation and other transformation processes, contributing to the development of more complex molecular structures.

  • 2-Methoxypyridin-3-amine  CAS:20265-38-7

    2-Methoxypyridin-3-amine CAS:20265-38-7

    2-Methoxypyridin-3-amine is an organic compound with the molecular formula C7H9N. It features a pyridine ring with a methoxy group (-OCH3) at the 2-position and an amine group (-NH2) at the 3-position. This compound serves as an important building block in synthetic organic chemistry, where its functional groups allow for various chemical transformations. Its unique structure provides potential biological activity, making it a subject of interest in medicinal chemistry.

  • 2-BROMO-3-FORMYLPYRIDINE CAS:128071-75-0

    2-BROMO-3-FORMYLPYRIDINE CAS:128071-75-0

    2-Bromo-3-formylpyridine is an organic compound with the molecular formula C6H4BrN and a structure featuring a pyridine ring with a bromine atom at the 2-position and a formyl group (-CHO) at the 3-position. This compound is of great interest in organic synthesis due to its reactive functional groups, which facilitate a variety of chemical transformations. The presence of these groups makes it a valuable building block for synthesizing more complex molecules in pharmaceutical and agrochemical research.

     

  • (2-Aminophenyl)boronic acid hydrochloride  CAS:863753-30-4

    (2-Aminophenyl)boronic acid hydrochloride CAS:863753-30-4

    (2-Aminophenyl)boronic acid hydrochloride is a boronic acid derivative with the molecular formula C6H8BClN. It features an amino group (-NH2) at the 2-position of a phenyl ring, along with a boronic acid functionality. The presence of the hydrochloride salt improves its solubility and stability in aqueous environments, making it suitable for various chemical applications. This compound is notable for its utility in organic synthesis and medicinal chemistry, where it serves as a key building block in the development of diverse bioactive molecules.

     

  • Methyl cinnamate CAS:103-26-4

    Methyl cinnamate CAS:103-26-4

    Methyl cinnamate is an ester formed from the reaction between cinnamic acid and methanol, characterized by a pleasant, sweet aroma often associated with fruits and flowers. This compound features a cinnamate moiety alongside a methyl group, providing it with distinctive properties that make it valuable in various applications. Methyl cinnamate is widely used in the flavor and fragrance industry as a flavoring agent and fragrance component. Additionally, it is explored for its potential therapeutic properties, including antioxidant and anti-inflammatory activities, making it a compound of interest in organic synthesis, nutritional science, and natural product chemistry.

     

  • 4-Biphenylacetonitrile CAS:31603-77-7

    4-Biphenylacetonitrile CAS:31603-77-7

    4-Biphenylacetonitrile, also known as 4-(biphenyl-4-yl)acetonitrile, is an organic compound characterized by a biphenyl structure attached to an acetonitrile group. This compound is notable for its aromatic features and the presence of the cyano (-C≡N) functional group, which enhances its reactivity and applicability in various chemical reactions. 4-Biphenylacetonitrile serves as a crucial intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its unique properties make it a subject of interest in material science, contributing to the creation of functionalized materials with potential applications across multiple industries.

  • Ethyl 3-phenylpropionate CAS:2021-28-5

    Ethyl 3-phenylpropionate CAS:2021-28-5

    Ethyl 3-phenylpropionate is an ester derived from the reaction of ethyl alcohol and 3-phenylpropanoic acid. This compound is characterized by the presence of a phenyl group attached to a three-carbon propionate chain. Ethyl 3-phenylpropionate is recognized for its pleasant, fruity aroma, making it a valuable flavoring and fragrance agent in the food and cosmetics industries. Additionally, it serves as a versatile building block in organic synthesis, participating in various chemical transformations to produce more complex molecules. Understanding its properties and applications is essential for researchers in organic chemistry and industrial applications.

  • 9-Anthracenemethanol CAS:1468-95-7

    9-Anthracenemethanol CAS:1468-95-7

    9-Anthracenemethanol, also known as 9-hydroxyanthracene, is an organic compound characterized by a hydroxymethyl group (-CH2OH) attached to the anthracene framework. This polycyclic aromatic hydrocarbon is notable for its unique structure, which imparts distinctive chemical and physical properties. 9-Anthracenemethanol serves as an important intermediate in organic synthesis and materials science, being utilized in the development of dyes, pharmaceuticals, and organic electronics. Its ability to participate in various chemical reactions makes it a valuable compound for creating functional materials with tailored properties, highlighting its relevance in both industrial applications and academic research.

  • Cinnamoyl chloride CAS:102-92-1

    Cinnamoyl chloride CAS:102-92-1

    Cinnamoyl chloride is an aromatic acyl chloride formed from cinnamic acid, featuring a carbonyl group (C=O) and a chlorine atom attached to a benzene ring with a propenyl side chain. This compound is significant in organic synthesis due to its reactivity as an acylating agent, which enables the introduction of cinnamoyl groups into various substrates. Cinnamoyl chloride is commonly used in the synthesis of pharmaceuticals, agrochemicals, and other functionalized organic compounds. Its ability to facilitate Friedel-Crafts acylation and other nucleophilic acyl substitution reactions makes it a valuable building block in synthetic organic chemistry.