Search

  • Order Status
  • Quick Order
  • Promos
Element SearchElement SearchStructure SearchStructure Search
(S)-(-)-2-Amino-2-methyl-4-pentenoic acid, 98%, ee 99+%
(S)-(-)-2-Amino-2-methyl-4-pentenoic acid, 98%, ee 99+%
(S)-(-)-2-Amino-2-methyl-4-pentenoic acid, 98%, ee 99+%
Thermo Scientific Chemicals

(S)-(-)-2-Amino-2-methyl-4-pentenoic acid, 98%, ee 99+%

CAS: 96886-55-4 | C6H11NO2 | 129.159 g/mol
Have Questions?
Change viewbuttonViewtableView
Quantity:
250 mg
1 g
ChemDexTry the chem dexTM web app
Catalog number H54922.03
also known as H54922-03
Price (USD)
479.00
Each
Quantity:
1 g
Request bulk or custom format
Price (USD)
479.00
Each
Chemical Identifiers
CAS96886-55-4
IUPAC Name2-amino-2-methylpent-4-enoic acid
Molecular FormulaC6H11NO2
InChI KeyQMBTZYHBJFPEJB-UHFFFAOYNA-N
SMILESCC(N)(CC=C)C(O)=O
View more
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to pale cream or pale yellow
FormPowder
Assay from Suppliers CofAEnantiomeric Excess (EE): ≥99.0%
Assay from Suppliers CofA≥97.5%
It is used in organic synthesis and as an pharmaceutical intermediate.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
It is used in organic synthesis and as an pharmaceutical intermediate.

Solubility
Very soluble in water.

Notes
Store at 4°C. Keep away from oxidizing agents and heat.
RUO – Research Use Only

General References:

  1. Quirinus B. Broxterman.; Bernard Kaptein.; Johan Kamphuis.; Hans E. Schoemaker. Synthesis of (optically active) sulfur-containing trifunctional amino acids by radical addition to (optically active) unsaturated amino acids. J. Org. Chem. 1992, 57 (23),6286-6294.
  2. Peng-Fei Xu.; Shuo Li.; Ta-Jung Lu .; Chen-Chang Wu.; Botao Fan.; Georgia Golfis. Asymmetric Synthesis of α,α-Disubstituted α-Amino Acids by Diastereoselective Alkylation of Camphor-Based Tricyclic Iminolactone. J. Org. Chem. 2006, 71 (12),4364-4373.