cas 1380336-01-5|| where to buy 1-Fmoc-4,4-dimethyl-L-proline

Product Name:1-Fmoc-4,4-dimethyl-L-proline

IUPAC Name:(2S)-1-{[(9H-fluoren-9-yl)methoxy]carbonyl}-4,4-dimethylpyrrolidine-2-carboxylic acid

: CAS：1380336-01-5; Molecular Formula：C22H23NO4; Purity：95%+

: Catalog Number：CM476917; Molecular Weight：365.43

Packing Unit	Available Stock	Price($)
CM476917-100mg	5-6 Weeks	ƀȬŴǕ
CM476917-250mg	5-6 Weeks	ƀɅƻȬ
CM476917-500mg	6-7 Weeks	ȁȁǕǕ
CM476917-1g	6-7 Weeks	ȁǕɅƀ

Inquiry: sales@chemenu.com

For R&D use only.

Inquiry Form

Chemical Name

CAS Number

Quantity*

Required Specifications*
(Assay %, Material Grade etc.)

Contact Name*

Contact Email*

Meanwhile I'd like to create a registered account on CHEMENU.COM with the above email.

I'd like to receive emails related to products with similar structures to 1380336-01-5 regularly via the above email.

Additional Notes

Verification code*

refresh

Product Details

: CAS NO:1380336-01-5; Molecular Formula:C22H23NO4; Melting Point:-; Smiles Code:CC1(C)C[C@H](N(C1)C(=O)OCC1C2=CC=CC=C2C2=C1C=CC=C2)C(O)=O; Density:

: Catalog Number:CM476917; Molecular Weight:365.43; Boiling Point:; MDL No:MFCD29277510; Storage:

Category Infos

: Pyrrolidines; Pyrrolidine, also known as tetrahydropyrrole, is a saturated five-membered heterocyclic ring, which is miscible with water. Pyrrolidine exists in many alkaloids and drug molecules, such as kappa opioids, antagonists of dopamine D4 receptors, and HIV reverse transcriptase inhibitors.

: Fluorenes; Fluorene is a polycyclic aromatic hydrocarbon insoluble in water and soluble in many organic solvents. Fluorenes are one of the most important fluorescent molecules with applications in polymers, electronic devices, sensors, and photochromic materials.

Product Other Information

Product Overview	1-Fmoc-4,4-dimethyl-L-proline is a chemical compound that has been widely used in scientific research due to its unique properties. It is a proline derivative that is commonly used in peptide synthesis, and it has been shown to have a wide range of biochemical and physiological effects.
Synthesis and Application	The synthesis of 1-Fmoc-4,4-dimethyl-L-proline involves several steps. The first step is the protection of the amine group with a Boc (tert-butyloxycarbonyl) group. The second step is the alkylation of the proline ring with 4,4-dimethyl-2-oxazoline. The third step is the deprotection of the Boc group, followed by the introduction of the Fmoc (9-fluorenylmethyloxycarbonyl) group. The final step is the deprotection of the Fmoc group to obtain the desired product. 1-Fmoc-4,4-dimethyl-L-proline has been widely used in scientific research as a building block for the synthesis of peptides. It is particularly useful in the synthesis of cyclic peptides due to its unique conformational properties. It has also been used in the synthesis of peptidomimetics, which are compounds that mimic the structure and function of peptides. Additionally, it has been used in the synthesis of bioactive peptides, which have potential applications in drug discovery and development.
Future Directions	There are several future directions for research on 1-Fmoc-4,4-dimethyl-L-proline. One potential area of research is the development of new synthetic methods for the compound. Additionally, further research is needed to fully understand the mechanism of action of 1-Fmoc-4,4-dimethyl-L-proline. This could lead to the development of new bioactive peptides and potential drug candidates. Finally, research is needed to explore the potential applications of 1-Fmoc-4,4-dimethyl-L-proline in the treatment of inflammatory diseases and other conditions.

Inquiry Form

Product Details

Category Infos

Related Products

Product Other Information