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ethyl N-((benzyloxy)carbonyl)-N-(2-methylallyl)glycinate
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- This compound serves as a versatile intermediate in peptide synthesis, medicinal chemistry, and chiral molecule synthesis.
ethyl N-((benzyloxy)carbonyl)-N-(2-oxopropyl)glycinate
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Category:
- This compound is a versatile intermediate in peptide synthesis, medicinal chemistry, and chiral molecule synthesis.
N-((benzyloxy)carbonyl)-N-(2-oxopropyl)glycine
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- The carboxylic acid functionality provides a versatile site for amide bond formation and other derivatizations.
dimethyl (R)-2-hydroxysuccinate
CAS No:
- 70681-41-3
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- Its chiral hydroxyl functionality allows for enantioselective transformations, making it valuable for synthesis of bioactive molecules, chiral ligands, and intermediates for active pharmaceutical ingredients (APIs).
dimethyl (R)-2-(benzyloxy)succinate
CAS No:
- 134356-95-9
Category:
- The benzyloxy group acts as a protecting group for the hydroxyl functionality, enabling selective transformations, while the R-chirality provides stereochemical control in downstream reactions.
(R)-2-(benzyloxy)succinic acid
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- This compound is a valuable intermediate in asymmetric synthesis, medicinal chemistry, and fine chemical production.
(S)-2-(benzyloxy)butane-1,4-diol
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- The benzyloxy group provides protection for the secondary alcohol, enabling selective transformations, while the S-chirality allows stereochemical control in downstream reactions.
(S)-(((1,4-diiodobutan-2-yl)oxy)methyl)benzene
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- The diiodo moiety allows for selective cross-coupling reactions (e.g., Suzuki, Sonogashira, Heck) and other halogen-based transformations.
(1S,3S)-3-(benzyloxy)-1-(p-tolyl)cyclopentane-1-carbonitrile
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- The benzyloxy group acts as a protecting group for the secondary alcohol, while the nitrile functionality is suitable for further transformations such as hydrolysis, amidation, or cyclization.
(1S,3S)-3-(benzyloxy)-1-phenylcyclopentane-1-carbonitrile
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- The benzyloxy group acts as a protecting group for the secondary alcohol, while the nitrile functionality allows for further functionalization, including hydrolysis, amidation, or cyclization.
2-(tert-butoxycarbonyl)-5-thia-2-azaspiro[3.4]octane-8-carboxylic acid 5,5-dioxide
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- This compound is a valuable intermediate in medicinal chemistry, peptide synthesis, and spirocyclic compound development.
tert-butyl 8-(((benzyloxy)carbonyl)amino)-5-thia-2-azaspiro[3.4]octane-2-carboxylate 5,5-dioxide
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Category:
- This compound is a highly versatile intermediate in peptide synthesis, medicinal chemistry, and spirocyclic drug development.