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![H-imidazo[1,5-a]pyridin-1-amine hydrochloride CAS:1519867-88-9](https://cdn.globalso.com/xindaobiotech/H@A6_8F9ZLLT0QCOA699.png)
H-imidazo[1,5-a]pyridin-1-amine hydrochloride CAS:1519867-88-9
H-imidazo[1,5-a]pyridin-1-amine hydrochloride is a chemically significant compound widely employed in pharmaceutical research and organic synthesis. This heterocyclic amine derivative possesses a fused imidazo-pyridine ring system, imparting unique structural and reactivity properties suitable for various chemical transformations. The hydrochloride salt form enhances its stability and solubility, making it a convenient reagent for medicinal chemistry applications. Chemists utilize this compound as a versatile building block for the synthesis of diverse molecular scaffolds and pharmaceutical intermediates, offering opportunities for innovative drug discovery and development.
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Methyl 5-amino-1H-indazole-3-carboxylate CAS:660411-95-0
Methyl 5-amino-1H-indazole-3-carboxylate is a chemically significant compound widely employed in organic synthesis and pharmaceutical research. This molecule contains an amino-indazole core linked to a carboxymethyl ester group, offering unique structural and reactivity properties suitable for diverse chemical transformations. The presence of the indazole scaffold imparts distinct aromaticity and functional diversity, making it valuable for medicinal chemistry applications. Chemists utilize this compound as a versatile building block for the synthesis of heterocyclic compounds and pharmaceutical intermediates, providing opportunities for innovative molecular design and exploration in the field of chemical sciences.
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4-Hydrazino-piperidine-1-carboxylic acid benzyl ester dihydrochloride CAS:916831-70-4
4-Hydrazino-piperidine-1-carboxylic acid benzyl ester dihydrochloride is a chemical compound commonly utilized in organic synthesis and medicinal chemistry. This dihydrochloride salt derivative of the benzyl ester of hydrazinopiperidine-1-carboxylic acid is recognized for its enhanced stability and solubility properties compared to the free base form. With a well-defined structure and unique functional groups, 4-Hydrazino-piperidine-1-carboxylic acid benzyl ester dihydrochloride serves as a valuable intermediate in the synthesis of pharmaceuticals and bioactive compounds.
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(S)-4-benzyloxymandelic acid CAS:197437-40-4
(S)-4-benzyloxymandelic acid is a valuable compound with applications in organic synthesis and the pharmaceutical industry. This chiral mandelic acid derivative features a benzyl ether moiety attached to the hydroxyl group at the 4-position, imparting unique stereochemical and reactivity properties. The S configuration of this compound defines its enantiomeric purity and influences its interactions in chemical reactions. Chemists and researchers utilize this compound as a key building block for the preparation of chiral compounds, pharmaceutical intermediates, and fine chemicals due to its synthetic versatility and chirality.
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5-Chloro-6-fluoro-1H-indazole CAS:1305207-97-9
5-Chloro-6-fluoro-1H-indazole is a chemical compound widely utilized in pharmaceutical research and organic synthesis. Belonging to the class of indazole derivatives, it is distinguished by its chloro and fluoro substituents on the indazole ring system. This compound is valued for its structural diversity and potential pharmacological properties. With high purity and stability, 5-Chloro-6-fluoro-1H-indazole serves as a key intermediate in the synthesis of various biologically active molecules and pharmaceutical candidates.
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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.
