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(R)-3-bromo-7-methyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine
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- he bromo substituent enables cross-coupling and functionalization reactions, while the tetrahydro ring and methyl group provide structural rigidity and chemical versatility.
(S)-3-bromo-7-methyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine
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- This compound is a valuable intermediate in medicinal chemistry and heterocyclic synthesis.
(S)-5-benzyl-3-bromo-7-methyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine
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- The bromo substituent allows for cross-coupling reactions, the benzyl group provides a handle for further derivatization, and the tetrahydro ring and methyl group offer structural rigidity.
(R)-5-benzyl-3-bromo-7-methyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine
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- The bromo substituent enables cross-coupling reactions, the benzyl group provides a handle for derivatization, and the tetrahydro ring and methyl group give structural rigidity.
methyl (S)-4-(5-benzyl-7-methyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazin-3-yl)benzoate
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- he benzoate moiety allows for further functionalization, while the tetrahydropyrazolo[1,5-a]pyrazine scaffold provides structural rigidity and stereochemical control.
4-bromo-1H-pyrazole-5-carbaldehyde
CAS No:
- 1007346-33-9
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- The aldehyde group allows for condensation, cyclization, and functional group transformations, while the bromo substituent enables cross-coupling reactions, making it useful for the synthesis of bioactive molecules, heterocyclic drugs, and agrochemical compounds.
methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
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- 171364-80-0
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- Its pinacol boronate functionality provides stability, reactivity, and ease of handling in organic synthesis.
(R)-2-(benzylamino)propan-1-ol
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- The chiral center allows for stereoselective synthesis, making it valuable in asymmetric transformations and drug discovery applications.
(S)-2-(benzylamino)propan-1-ol
CAS No:
- 6940-80-3
Category:
- The S-chirality allows for stereoselective synthesis, making it valuable in asymmetric transformations and drug discovery applications.
tert-butyl (S)-3-(4-(methoxycarbonyl)phenyl)-7-methyl-6,7-dihydropyrazolo[1,5-a]pyrazine-5(4H)-carboxylate
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- This compound is a key intermediate in medicinal chemistry, particularly for the synthesis of bioactive molecules, enzyme inhibitors, and chiral drug candidates.
benzyl (3R,8aS)-3-(hydroxymethyl)-8a-methyl-5-oxohexahydro-7H-oxazolo[3,2-a]pyrazine-7-carboxylate
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- Its well-defined stereochemistry makes it valuable for the synthesis of bioactive molecules, peptide mimetics, and drug candidates.
ethyl (tert-butoxymethyl)glycinate
CAS No:
- 14719-37-0
Category:
- The BOM protecting group provides stability and selective deprotection options, while the ethyl ester allows for further chemical transformations, including amidation or peptide coupling reactions.