Fmoc-4-tert-butoxy-L-proline丨CAS 122996-47-8

Fmoc-4-tert-butoxy-L-proline丨CAS 122996-47-8
Product Introduction:
Catalog No.: SS098251
CAS No.: 122996-47-8
Purity(LCMS): 98%min
Product Name: Fmoc-4-tert-butoxy-L-proline
Molecular Formula: C24H27NO5
Molecular Weight: 409.47
Synonym(s): (2S,4R)-4-(tert-butoxy)-1-{[(9H-fluoren-9-yl)methoxy]carbonyl}pyrrolidine-2-carboxylic acid
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Technical Parameters
Description

Hangzhou Leap Chem Co., Ltd. is one of the most professional manufacturers and suppliers of fmoc-4-tert-butoxy-l-proline丨cas 122996-47-8 in China. Welcome to wholesale bulk high quality chemical products at competitive price from our factory. If you have any enquiry about custom service, please feel free to email us.

 

Specifications

 

Appearance

White to off-white powder

Purity (LCMS)

98% min

NMR

comply to structure

Optical rotation

25±2.5 deg

 

Transport Information

 

Parameter

Specification

UN Number

 

Class

 

Packing Group

 

H.S. Code

2933990099306

Stability & Reactivity

The product is chemically stable under standard ambient conditions.

Storage

Tightly closed. Dry. 2-8degC

Condition to Avoid

 

Package

 

 

Manufacturing Information

 

Parameter

Specification

Capacity

100kg/month

Frequency

 

Main Export Countries

 

Capacity/Batch

 

Experience

Production since 2015

Stock

 

 

 

 

Applications of Fmoc-4-tert-butoxy-L-proline丨CAS 122996-47-8

1. Peptide Synthesis

Primarily used as a protected amino acid building block in solid-phase peptide synthesis (SPPS).

The Fmoc (9-fluorenylmethoxycarbonyl) group protects the amino function during peptide chain elongation, allowing selective deprotection.

The 4-tert-butoxy modification on the proline side chain enhances solubility and can influence the peptide's conformational properties.

Useful for synthesizing peptides with specific structural or functional requirements, including cyclic peptides and constrained conformations.

2. Pharmaceutical and Biochemical Research

Employed in the design and synthesis of bioactive peptides and peptidomimetics for drug discovery.

Helps generate peptides with improved stability, bioavailability, or target specificity.

3. Chemical Biology

Used to incorporate modified proline residues into peptides, which can affect protein folding, receptor binding, and biological activity.

Facilitates studies on the role of proline derivatives in protein structure and function.


 

Benefits

✅ Selective Protection

The Fmoc protecting group is base-labile, allowing easy removal under mild conditions without affecting other sensitive groups.

✅ Enhanced Peptide Stability

The tert-butoxy group on proline can improve peptide solubility and modulate conformation, influencing biological activity.

✅ Facilitates Complex Peptide Design

Enables the incorporation of modified proline residues to fine-tune peptide structure and function.

✅ Widely Compatible with SPPS Protocols

Compatible with standard Fmoc-based solid-phase synthesis techniques used in research and industry.


 

Summary

Fmoc-4-tert-butoxy-L-proline丨CAS 122996-47-8 is a specialized Fmoc-protected amino acid derivative used extensively in solid-phase peptide synthesis. Its combination of an Fmoc protecting group and a tert-butoxy-modified proline residue makes it valuable for producing peptides with enhanced stability and tailored conformations, supporting research in pharmaceuticals, biochemistry, and chemical biology.

 

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