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N-Methyl-N-(tetrahydrofuran-3-ylmethyl)amine CAS:7179-93-3
N-Methyl-N-(tetrahydrofuran-3-ylmethyl)amine is a chemical compound with diverse potential applications in pharmaceutical research and organic synthesis. This molecule combines a tetrahydrofuran ring substituted with a methyl group and an amine functional group, offering unique structural features that can influence its reactivity and biological properties. The presence of the N-methyl group enhances its stability and solubility characteristics, making it suitable for various laboratory and medicinal chemistry applications. Researchers can leverage its versatile structure to explore new synthetic pathways or investigate its interactions with biological targets.
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![4-Chloro-2-(trifluoromethyl)pyrazolo[1,5-a]pyrazine CAS:877402-79-4](https://cdn.globalso.com/xindaobiotech/14Z4YR3PJ6@V5_YM193.png)
4-Chloro-2-(trifluoromethyl)pyrazolo[1,5-a]pyrazine CAS:877402-79-4
4-Chloro-2-(trifluoromethyl)pyrazolo[1,5-a]pyrazine is a heterocyclic compound with potential applications in medicinal chemistry and materials science. This molecule features a fused pyrazine ring system substituted with a chlorine atom and a trifluoromethyl group, imparting unique structural and chemical properties. The compound’s aromatic nature and fluorinated substituent make it an intriguing scaffold for designing biologically active molecules or functional materials. Its structural complexity offers opportunities for exploring diverse chemical transformations and molecular interactions.
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![2-(Trifluoromethyl)pyrazolo[1,5-a]pyrazin-4-ol CAS:877402-82-9](https://cdn.globalso.com/xindaobiotech/VYH6FUCIIBE_I7B6OOPY158.png)
2-(Trifluoromethyl)pyrazolo[1,5-a]pyrazin-4-ol CAS:877402-82-9
2-(Trifluoromethyl)pyrazolo[1,5-a]pyrazin-4-ol is a heterocyclic compound with potential applications in medicinal chemistry and organic synthesis. This molecule contains a pyrazolo[1,5-a]pyrazine core decorated with a trifluoromethyl group and a hydroxyl moiety at the 4-position, offering unique structural features that can influence its reactivity and biological properties. The compound’s aromatic nature and functional groups make it an intriguing scaffold for designing biologically active molecules or studying structure-activity relationships. Its structural complexity provides opportunities for exploring diverse chemical transformations and molecular interactions.
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tert-butyl 3-amino-4-cyanopyrrolidine-1-carboxylate CAS:1305712-89-3
tert-Butyl 3-amino-4-cyanopyrrolidine-1-carboxylate is a chemical compound with diverse applications in organic synthesis and pharmaceutical research. This molecule contains a pyrrolidine ring substituted with an amino group at the 3-position, a cyano group at the 4-position, and a tert-butyl ester at the carboxylic acid moiety. The compound’s unique structure provides opportunities for exploring its reactivity in various chemical transformations and its potential biological activities. Its versatility makes it a valuable building block for designing novel molecules or investigating synthetic pathways.
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(S)-tert-Butyl3-(2-hydroxyethyl)piperazine-1-carboxylate CAS:1273577-11-9
(S)-tert-Butyl 3-(2-hydroxyethyl)piperazine-1-carboxylate is a chiral compound with diverse applications in organic synthesis and pharmaceutical research. This molecule features a piperazine ring substituted with a 2-hydroxyethyl group at the 3-position and a tert-butyl ester at the carboxylic acid moiety in an S-stereoisomeric configuration. The compound’s chiral center and functional groups offer unique structural properties that can influence its reactivity and biological activities. Its stereochemistry and functional groups make it a valuable building block for designing bioactive molecules or investigating stereocontrolled chemical reactions.
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Methyl 3-amino-2-(aminomethyl)propanoate dihydrochloride CAS:440644-06-4
Methyl 3-amino-2-(aminomethyl)propanoate Dihydrochloride is a chemical compound commonly used as a building block in organic synthesis and pharmaceutical research. This molecule consists of a propanoic acid derivative with an amino group at the 3-position and an aminomethyl group at the 2-position, forming a dihydrochloride salt for enhanced stability and solubility. The compound’s structure offers versatility for creating diverse molecular structures or investigating synthetic pathways due to its reactive functional groups and stability as a salt.
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1-(4-Chloro-phenyl)-5-oxo-pyrrolidine-3-carboxylic acid CAS:39629-87-3
1-(4-Chloro-phenyl)-5-oxo-pyrrolidine-3-carboxylic acid is a chemical compound with significant applications in organic synthesis and pharmaceutical research. This molecule consists of a pyrrolidine ring substituted with a 4-chlorophenyl group at the 1-position and a carboxylic acid functionality at the 3-position. The compound’s structure offers opportunities for diverse molecular modifications and synthetic pathways due to its aromatic group and reactive carboxylic acid moiety, providing versatility for creating various derivatives or exploring chemical transformations.
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tert-Butyl 4-(1-aminopropan-2-yl)piperazine-1-carboxylate CAS:1018248-96-8
tert-Butyl 4-(1-aminopropan-2-yl)piperazine-1-carboxylate is a chemical compound with applications in organic synthesis and pharmaceutical research. This molecule features a piperazine ring substituted with an aminopropan-2-yl group at the 4-position and a tert-butyl ester at the carboxylic acid moiety. The compound’s structure offers versatility for creating diverse molecular structures or exploring synthetic pathways due to its reactive functional groups. Its incorporation in synthetic schemes enables the construction of complex molecules for various research or industrial purposes.
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![6-Chlorothiazolo[4,5-b]pyridine CAS:1780572-16-8](https://cdn.globalso.com/xindaobiotech/V3@A6KDXTE0I05WML119.png)
6-Chlorothiazolo[4,5-b]pyridine CAS:1780572-16-8
6-Chlorothiazolo[4,5-b]pyridine is a heterocyclic compound with potential applications in medicinal chemistry and organic synthesis. This molecule features a fused thiazole and pyridine ring system, with a chlorine atom at the 6-position, imparting unique structural and chemical properties. The compound’s aromatic nature and nitrogen-containing rings make it an interesting scaffold for designing biologically active molecules or functional materials. Its structural complexity offers opportunities for exploring diverse chemical transformations and molecular interactions.
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Di-tert-butyl cyclohexane-1,4-diyldicarbamate CAS:960071-19-6
Di-tert-butyl cyclohexane-1,4-diyldicarbamate is a chemical compound with potential applications in organic synthesis and materials science. This molecule consists of a cyclohexane-1,4-diyldicarbamate core decorated with tert-butyl groups, imparting sterically hindered properties that can influence its reactivity and stability. The compound’s structural features make it a versatile building block for creating complex organic molecules or functional materials. Its unique composition offers opportunities for exploring diverse chemical transformations and designing novel compounds with tailored properties.
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tert-butyl (1R,2S)-2-(3-bromophenyl)cyclopropylcarbamate CAS:1314323-97-1
tert-butyl (1R,2S)-2-(3-bromophenyl)cyclopropylcarbamate is a chiral compound with potential applications in medicinal chemistry and organic synthesis. This molecule comprises a cyclopropyl ring substituted with a 3-bromophenyl group and a carbamate functional group protected by a tert-butyl moiety in a defined stereochemical configuration. The compound’s chiral centers and aromatic substituent offer unique structural features that can influence its reactivity and biological activities. Its stereochemistry and functional groups make it a valuable precursor for designing bioactive molecules or exploring stereocontrolled chemical transformations.
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(S)-5-Phenylmorpholin-3-one CAS:1052209-96-7
(S)-5-Phenylmorpholin-3-one is a chiral compound with potential applications in medicinal chemistry and pharmaceutical research. This molecule comprises a morpholine ring substituted with a phenyl group, featuring a chiral center that imparts stereochemical properties important for biological activity. The compound’s structural arrangement offers opportunities for exploring its interaction with biological targets or enzymatic systems, making it valuable for drug discovery studies and chemical biology investigations.
