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CAS 95715-87-0

:

(R)-Garner aldehyde

Description:
(R)-Garner aldehyde, with the CAS number 95715-87-0, is a chiral organic compound characterized by its unique structure and properties. It is primarily recognized for its role in organic synthesis, particularly in the preparation of various pharmaceuticals and biologically active molecules. The compound features a specific stereochemistry, which is crucial for its reactivity and interaction with biological systems. As an aldehyde, it contains a carbonyl group (C=O) at the terminal position of a carbon chain, contributing to its reactivity in nucleophilic addition reactions. (R)-Garner aldehyde is often utilized in asymmetric synthesis due to its ability to influence the stereochemical outcome of reactions. Its physical properties, such as boiling point and solubility, are typical of aldehydes, making it a versatile intermediate in synthetic organic chemistry. Additionally, the compound's chirality allows for the exploration of enantioselective reactions, which are essential in the development of enantiomerically pure compounds in medicinal chemistry.
Formula:C11H19NO4
InChI:InChI=1S/C11H19NO4/c1-10(2,3)16-9(14)12-8(6-13)7-15-11(12,4)5/h6,8H,7H2,1-5H3/t8-/m0/s1
InChI key:InChIKey=PNJXYVJNOCLJLJ-QMMMGPOBSA-N
SMILES:C(OC(C)(C)C)(=O)N1[C@@H](C=O)COC1(C)C
Synonyms:
  • (4R)-4-Formyl-2,2-dimethyl-1,3-oxazolidine-3-carboxylic acid tert-butyl ester
  • (R)-(+)-3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde
  • (R)-(+)-3-tert-Butoxycarbonyl-2,2-dimethyloxazolidine-4-carboxaldehyde
  • (R)-2,2-Dimethyl-3-tert-butoxycarbonyl-1,3-oxazolidine-4-carboxaldehyde
  • (R)-3-tert-Butoxycarbonyl-2,2-dimethyl-4-formyloxazolidine
  • (R)-4-Formyl-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester
  • (R)-Garner aldehyde
  • (R)-Garner's aldehyde
  • (R)-tert-Butyl 4-formyl-2,2-dimethyloxazolidine-3-carboxylate
  • (S)-3-N-Boc-aminopyrrolidine
  • See more synonyms
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Purity (%)
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100
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0
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50
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90
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100
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