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Catalog Number:
39650
CAS Number:
108149-60-6
(S)-(-)-3-tert-Butoxycarbonyl-4-methoxycarbonyl-2,2-dimethyl-1,3-oxazolidine
Purity:
≥ 98.5% (Chiral purity)
Synonym(s):
(S)-(-)-3-Boc-4-methoxycarbonyl-2,2-dimethyl-1,3-oxazolidine, Methyl (S)-(-)-3-tert-Butoxycarbonyl-2,2-dimethyl-4-oxazolidinecarboxylate
Hazmat
Documents
$43.87 /1G
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Product Information
Synonyms
(S)-(-)-3-Boc-4-methoxycarbonyl-2,2-dimethyl-1,3-oxazolidine, Methyl (S)-(-)-3-tert-Butoxycarbonyl-2,2-dimethyl-4-oxazolidinecarboxylate
CAS Number
108149-60-6
Purity
≥ 98.5% (Chiral purity)
Molecular Formula
C12H21NO5
Molecular Weight
0
MDL Number
MFCD00192279
PubChem ID
5138497
Density
1.08 g/mL at 25 °C
Appearance
Colorless to slightly yellow liquid
Boiling Point
101 - 102 °C / 2 mmHg (Lit.)
Refractive Index
n20D 1.44
Optical Rotation
[α]20D = −55 +/- 2 ° (C = 1.3 in Chloroform)
Conditions
Store at RT
General Information
Synonyms
(S)-(-)-3-Boc-4-methoxycarbonyl-2,2-dimethyl-1,3-oxazolidine, Methyl (S)-(-)-3-tert-Butoxycarbonyl-2,2-dimethyl-4-oxazolidinecarboxylate
CAS Number
108149-60-6
Purity
≥ 98.5% (Chiral purity)
Molecular Formula
C12H21NO5
Molecular Weight
0
MDL Number
MFCD00192279
PubChem ID
5138497
Density
1.08 g/mL at 25 °C
Appearance
Colorless to slightly yellow liquid
Boiling Point
101 - 102 °C / 2 mmHg (Lit.)
Refractive Index
n20D 1.44
Optical Rotation
[α]20D = −55 +/- 2 ° (C = 1.3 in Chloroform)
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-(-)-3-tert-Butoxycarbonyl-4-methoxycarbonyl-2,2-dimethyl-1,3-oxazolidine is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs that target neurological disorders.
  • Peptide Synthesis: It is used in the solid-phase synthesis of peptides, enhancing the efficiency and yield of the process, which is crucial for producing therapeutic proteins.
  • Chiral Auxiliary: The compound acts as a chiral auxiliary in asymmetric synthesis, allowing chemists to produce enantiomerically pure compounds, which are vital in drug formulation.
  • Research in Organic Chemistry: It provides a versatile framework for the exploration of new synthetic pathways and methodologies, aiding researchers in discovering novel compounds.
  • Bioconjugation Techniques: This chemical is employed in bioconjugation strategies, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in diagnostics and therapeutics.

Citations