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2-Formylfuran-5-boronic acid CAS:27329-70-0
2-Formylfuran-5-boronic acid is a chemical compound characterized by its boronic acid group attached to a furan ring with a formyl substituent. It is utilized in organic synthesis as a versatile building block due to its ability to form stable boronate esters and its reactivity in cross-coupling reactions. The compound’s structure facilitates its integration into various molecular frameworks, making it valuable in pharmaceutical and agrochemical research.
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1,2,3-triacetyl-5-deoxy-β-D-Ribose CAS:62211-93-2
1,2,3-Triacetyl-5-deoxy-β-D-ribose is a chemical compound with the molecular formula C14H18O7. It is characterized by a ribose sugar structure with three acetyl groups attached to the hydroxyl groups at positions 1, 2, and 3. This compound is significant in organic chemistry and pharmaceutical research due to its utility as a protective group for the ribose moiety in nucleoside synthesis and as a precursor in the preparation of nucleotide analogs.
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(2S,3S,5S)-5-(Tert-butyloxycarbonyl)amino-2-amino-3-hydroxy-1,6-diphenyl hexane (BDH Pure) CAS:144163-85-9
BDH Pure, or (2S,3S,5S)-5-(tert-butyloxycarbonyl)amino-2-amino-3-hydroxy-1,6-diphenyl hexane, is a compound utilized in biochemical and pharmaceutical research. It features a unique molecular structure that contributes to its applications in peptide chemistry and drug development.
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2′,3′-Di-O-acetyl-5′-deoxy-5-fuluro-D-cytidine CAS:161599-46-8
2′,3′-Di-O-acetyl-5′-deoxy-5-fluoro-D-cytidine is a chemical compound with the molecular formula C13H16FN3O6. It is characterized by a cytidine core with acetyl groups attached to the 2′ and 3′ positions and a fluorine substitution at the 5′ position of the ribose sugar. This compound is significant in nucleoside chemistry and pharmaceutical research due to its potential applications in antiviral and anticancer drug development.
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Trans-1,2-diaminocyclohexane CAS:1121-22-8
Trans-1,2-diaminocyclohexane is a chemical compound with the molecular formula C6H14N2. It consists of a cyclohexane ring with two amino groups (-NH2) attached to adjacent carbon atoms in a trans configuration. This compound is notable in organic chemistry and pharmaceutical research due to its structural versatility and applications in ligand design for metal complex catalysis and as a building block for biologically active compounds.
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(2S,3S,5S)-2-Amino-3-hydroxy-5-(tert-butyloxycarbonyl)amino-1,6-diphenyl-hexane hemi succinic acid salt(BDH succinic acid salt) CAS:183388-64-9
BDH succinic acid salt, or (2S,3S,5S)-2-Amino-3-hydroxy-5-(tert-butyloxycarbonyl)amino-1,6-diphenyl-hexane hemi succinic acid salt, is a compound used in pharmaceutical research and development. It possesses unique chemical properties that make it valuable in studies related to amino acid derivatives and peptide synthesis.
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(1R,2R)-(-)-1,2- diaminocyclohexane acid CAS:20439-47-8
(1R,2R)-(-)-1,2-diaminocyclohexane acid is a chemical compound with the molecular formula C6H14N2O2. It is characterized by a cyclohexane ring with two amino groups (-NH2) attached to adjacent carbon atoms (1R,2R configuration) and a carboxylic acid group (-COOH) on another carbon atom. This compound is significant in organic chemistry and pharmaceutical research due to its potential as a chiral building block in the synthesis of biologically active compounds and as a ligand in asymmetric catalysis.
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Fluorocytosine CAS:2022-85-7
Fluorocytosine, also known as 5-fluorocytosine, is a chemical compound with the molecular formula C4H4FN3O. It is characterized by the substitution of a fluorine atom at the 5 position of the cytosine molecule. Fluorocytosine is a nucleoside analog that has shown activity against certain fungal infections, particularly those caused by Candida species. Its mechanism of action involves disrupting fungal RNA and protein synthesis, making it a valuable antifungal agent in clinical settings.
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1,1-cyclobutanedicarboxylic CAS:5445-51-2
1,1-Cyclobutanedicarboxylic acid is a chemical compound with the molecular formula C6H8O4. It consists of a cyclobutane ring with two carboxylic acid (-COOH) groups attached to adjacent carbon atoms. This compound is notable in organic chemistry due to its unique strained ring structure, which influences its reactivity and applications in synthetic chemistry.
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3-AMINOPHTHALIC ACID HYDROCHLORIDE CAS:6946-22-1
3-Aminophthalic acid hydrochloride is a chemical compound recognized for its versatile applications in organic synthesis and materials science. This compound is synthesized through the reaction of 3-nitrophthalic acid with ammonia or an amine, followed by hydrochloric acid treatment to obtain the hydrochloride salt. It exhibits distinctive structural features that contribute to its functional diversity and potential applications across various fields.
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(S)-1-(3-Ethoxy-4-Methoxyphenyl)-2-(Methylsulfonyl)ethylaMine N-acetyl-L-leucine salt CAS:608141-43-1
(S)-1-(3-Ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethylamine N-acetyl-L-leucine salt is a chemical compound known for its diverse applications in organic synthesis and medicinal chemistry. This compound is synthesized through the reaction of (S)-1-(3-ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethanone with ammonia or an amine, followed by salt formation with N-acetyl-L-leucine. It exhibits distinctive structural features that contribute to its functional versatility and potential pharmacological activities.
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3-Quinuclidinol CAS:1619-34-7
3-Quinuclidinol, also known as quinuclidinol, is a significant compound in organic chemistry and pharmaceutical research due to its structural uniqueness and versatile applications. This chiral compound is derived from quinuclidine and exhibits distinct chemical and pharmacological properties that have attracted attention across various scientific disciplines.
