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tert-butyl ((tetrahydrofuran-3-yl)methyl)carbamate CAS:1487925-72-3
Tert-butyl ((tetrahydrofuran-3-yl)methyl)carbamate is a chemical compound widely used in organic synthesis and medicinal chemistry. It is characterized by its tert-butyl group attached to a tetrahydrofuran-3-ylmethyl moiety, offering unique reactivity and structural properties. This compound is valued for its stability and versatility in building complex molecules for various applications. With its well-defined structure intermediate and purity, tert-butyl ((tetrahydrofuran-3-yl)methyl)carbamate serves as a valuable in the synthesis of pharmaceuticals and agrochemicals.
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![6-Chloro-1H-benzo[d]imidazole-4-carboxylicacid CAS:180569-27-1](https://cdn.globalso.com/xindaobiotech/1K37N24IWHVCSAAU383348.png)
6-Chloro-1H-benzo[d]imidazole-4-carboxylicacid CAS:180569-27-1
6-Chloro-1H-benzo[d]imidazole-4-carboxylic acid is a compound with diverse applications in medicinal chemistry and materials science. Its benzimidazole core, featuring a chlorine substitution at the 6-position and a carboxylic acid functional group at the 4-position, endows it with unique properties suitable for various synthetic pathways. This molecule serves as a valuable building block for the synthesis of biologically active compounds and functional materials due to its structural versatility and synthetic accessibility. Researchers and chemists utilize this compound to explore new avenues in drug discovery, material science, and organic synthesis.
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5-amino-1H-indazole-3-carboxylic acid CAS:78155-77-8
5-amino-1H-indazole-3-carboxylic acid is a chemically significant compound with versatile applications in organic synthesis and medicinal chemistry. This molecule features an amino-indazole core attached to a carboxylic acid group, imparting unique structural and reactivity properties suitable for various chemical transformations. The presence of the indazole scaffold provides aromaticity and functional diversity, making it valuable for medicinal chemistry applications. Chemists utilize this compound as a key building block for the synthesis of heterocyclic compounds and pharmaceutical intermediates, offering opportunities for innovative molecular design and exploration in chemical sciences.
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1-((1S,2S)-2-(3-bromophenyl)cyclopropyl)ethanone CAS:2165532-10-3
1-((1S,2S)-2-(3-bromophenyl)cyclopropyl)ethanone is a chemically significant compound utilized in organic synthesis and medicinal chemistry. This molecule features a cyclopropyl-ethanone framework attached to a (1S,2S)-2-(3-bromophenyl) moiety, imparting unique structural and reactivity properties suitable for diverse chemical transformations. The presence of the cyclopropyl group and the bromophenyl substituent contributes to its synthetic versatility and functional diversity. Chemists employ this compound as a valuable building block for the synthesis of complex molecules and pharmaceutical intermediates, offering opportunities for innovative molecular design and exploration in chemical sciences.
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methyl 3-(benzylamino)-2-((benzylamino)methyl)propanoate dihydrochloride CAS:1243306-84-4
Methyl 3-(benzylamino)-2-((benzylamino)methyl)propanoate dihydrochloride is a chemical compound widely employed in organic synthesis and pharmaceutical research. This dihydrochloride salt derivative of methyl 3-(benzylamino)-2-((benzylamino)methyl)propanoate offers enhanced stability and solubility compared to its free base form. With a complex structure containing benzylamino and propanoate moieties, this compound serves as a valuable intermediate in the synthesis of bioactive molecules and drug candidates, characterized by its versatility and reactivity.
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(S)-4-hydroxymandelic acid CAS:13244-75-2
(S)-4-hydroxymandelic acid is a chemically significant compound with versatile applications in organic synthesis and pharmaceutical research. This chiral molecule, derived from mandelic acid, features a hydroxyl group at the 4-position, imparting unique reactivity and stereochemical properties. The (S) configuration ensures specific stereochemistry, making it valuable for chiral applications and asymmetric synthesis. This compound serves as a crucial building block for the preparation of chiral intermediates and pharmaceuticals, offering opportunities for innovative molecular design and exploration in chemical sciences.
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(S)-tert-butyl 5-(hydroxymethyl)-2,2-dimethylmorpholine-4-carboxylate CAS:1263078-18-7
(S)-tert-butyl 5-(hydroxymethyl)-2,2-dimethylmorpholine-4-carboxylate is a structurally unique compound with versatile applications in organic synthesis and pharmaceutical research. The chiral nature of the tert-butyl ester derivative at the 4-position, combined with the hydroxymethyl functionality on the 5th carbon of the morpholine ring, confers distinctive stereochemical properties suitable for diverse chemical transformations. This molecule serves as a valuable building block for the preparation of chiral intermediates and complex molecules due to its synthetic accessibility and chirality, offering opportunities for innovative molecular design and exploration in chemical sciences.
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Trans-tert-Butyl ((2-hydroxycyclopentyl)methyl)carbamate CAS:1354957-79-1
Trans-tert-Butyl ((2-hydroxycyclopentyl)methyl)carbamate is a chemical compound commonly utilized in organic synthesis and pharmaceutical research. This molecule, characterized by its tert-butyl group and carbamate functionality, exhibits unique reactivity and potential pharmacological properties. As a key intermediate in the synthesis of bioactive compounds, Trans-tert-Butyl ((2-hydroxycyclopentyl)methyl)carbamate offers versatility and structural diversity, making it valuable for medicinal chemistry applications.
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(R)-4-(tert-Butoxycarbonyl)-6,6-dimethylmorpholine-3-carboxylic acid CAS:1263077-92-4
(R)-4-(tert-Butoxycarbonyl)-6,6-dimethylmorpholine-3-carboxylic acid is a valuable compound with significant utility in organic synthesis and pharmaceutical research. Its chiral morpholine core, bearing a tert-butoxycarbonyl (Boc) protecting group at the 4-position and a carboxylic acid functionality at the 3-position, imparts unique stereochemical and reactivity properties. This molecule serves as a crucial intermediate for the synthesis of chiral building blocks and pharmaceutical intermediates, enabling the construction of complex molecular architectures with defined stereochemistry. Researchers and chemists utilize this compound to facilitate asymmetric synthesis and access enantiomerically pure compounds for drug discovery and materials science applications.
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(1H-Indol-3-yl)acetaldoxime CAS:2776-06-9
(1H-Indol-3-yl)acetaldoxime is a chemically significant compound with diverse applications in organic synthesis and chemical biology. This oxime derivative features an indole ring system connected to an acetaldoxime moiety, combining aromatic properties with oxime functionality. The presence of the indole scaffold imparts distinctive electronic and structural characteristics, making this compound valuable for various synthetic transformations and biological studies. (1H-Indol-3-yl)acetaldoxime serves as a versatile building block for the synthesis of heterocyclic compounds and molecular probes, offering opportunities for innovative molecular design and exploration in chemical sciences.
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(3S,4S)-1-Benzyl-4-(hydroxymethyl)pyrrolidin-3-ol CAS:849935-80-4
(3S,4S)-1-Benzyl-4-(hydroxymethyl)pyrrolidin-3-ol is a chemically significant compound with versatile applications in organic synthesis and medicinal chemistry. The stereochemistry of this pyrrolidine derivative, featuring (3S,4S) configuration, defines its unique structural and reactivity properties. The benzyl group at the 1-position and the hydroxymethyl moiety at the 4-position contribute to its synthetic versatility and functional diversity. This compound serves as a valuable building block for the synthesis of complex molecules and pharmaceutical intermediates, offering opportunities for innovative molecular design and exploration in chemical sciences.
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(R)-6,6-Dimethyl-morpholine-3-carboxylic acid hydrochloride CAS:1313277-22-3
(R)-6,6-Dimethyl-morpholine-3-carboxylic acid hydrochloride is a chemically significant compound used in pharmaceutical and organic synthesis. The (R) enantiomer configuration of this morpholine derivative ensures its precise stereochemistry, making it valuable for chiral applications. Its hydrochloride salt form enhances solubility and stability, facilitating its use in various reactions. This compound serves as an essential building block for the synthesis of chiral molecules with specific biological activities and structural properties, offering versatility and reliability in complex chemical transformations.
