CAS 135673-97-1

(S)-N-FMOC-Amino-2-cyclohexyl-propanoic acid

Description:

(S)-N-FMOC-Amino-2-cyclohexyl-propanoic acid is a synthetic amino acid derivative characterized by its unique structural features, which include a cyclohexyl group and a fluorenylmethyloxycarbonyl (FMOC) protecting group. The FMOC group is commonly used in peptide synthesis to protect the amino group, allowing for selective reactions at other functional sites. This compound is typically utilized in the field of organic chemistry and peptide synthesis due to its ability to facilitate the formation of peptide bonds while maintaining stability during the synthesis process. The presence of the cyclohexyl moiety contributes to the compound's hydrophobic characteristics, influencing its solubility and interaction with other molecules. Additionally, the stereochemistry indicated by the (S) configuration suggests that this compound exhibits specific spatial arrangements that can affect its biological activity and interactions. Overall, (S)-N-FMOC-Amino-2-cyclohexyl-propanoic acid serves as a valuable building block in the development of peptides and other bioactive compounds.

Formula: C₂₄H₂₇NO₄

Synonyms:

• Fmoc-L-cyclohexylalanine
• Fmoc-.beta.-cyclohexyl-Ala-OH
• Fmoc-Cha-OH
• (S)-N-(9-Fluorenylmethoxycarbonyl)-alpha-cyclohexyl-L-alanine
• N-alpha-(9-fluorenylmethyloxycarbonyl)-L-cyclohexylalanine
• Fmoc-(S)-3-Cyclohexylalanine

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-cyclohexyl-L-alanine

CAS: 135673-97-1

Formula: C₂₄H₂₇NO₄

Purity: >98.0%(T)(HPLC)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 393.48

Ref: 3B-F0857

N-Fmoc-3-cyclohexyl-L-alanine, 98%

CAS: 135673-97-1

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 Sci

Formula: C₂₄H₂₇NO₄

Purity: 98%

Molecular weight: 393.48

Ref: 02-H63910

Fmoc-β-cyclohexyl-Ala-OH

CAS: 135673-97-1

Bachem ID: 4018171.

Formula: C₂₄H₂₇NO₄

Purity: 99.86%

Color and Shape: White Powder

Molecular weight: 393.48

Ref: 01-4018171

Cyclohexanepropanoic acid,a-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (aS)-

CAS: 135673-97-1

Formula: C₂₄H₂₇NO₄

Purity: 97%

Color and Shape: Solid

Molecular weight: 393.4755

Ref: IN-DA00HUBP

Fmoc-(S)-3-Cyclohexylalanine

CAS: 135673-97-1

Fmoc-(S)-3-Cyclohexylalanine

Formula: C₂₄H₂₇NO₄

Purity: 99%

Color and Shape: white to off-white solid

Molecular weight: 393.48g/mol

Ref: 54-OR960948

Fmoc-Cha-OH

CAS: 135673-97-1

Formula: C₂₄H₂₇NO₄

Purity: ≥ 98.0%

Color and Shape: White to faint yellow or beige powder

Molecular weight: 393.48

Ref: 7W-GM6924

Fmoc-Cha-OH

CAS: 135673-97-1

Fmoc-Cha-OH (Fmoc-L-cyclohexylalanine) is an alanine derivative containing an Fmoc protecting group, which can be used for peptide synthesis and drug design.

Formula: C₂₄H₂₇NO₄

Purity: 99.71%

Color and Shape: Solid

Molecular weight: 393.48

Ref: TM-T66694

Fmoc-Cha-OH

CAS: 135673-97-1

M06091 - Fmoc-Cha-OH

Formula: C₂₄H₂₇NO₄

Purity: 97%

Color and Shape: Solid, White - Almost white powder

Molecular weight: 393.483

Ref: 10-M06091

Fmoc-Cha-OH

CAS: 135673-97-1

Fmoc-Cha-OH is an activated, histidine building block that is used to synthesize biomolecules such as proteins and peptides. It has been shown to modulate the activity of acidic phospholipases in inflammatory diseases, specifically colorectal carcinoma. This building block can be used for solid-phase synthesis, and has a high chemical stability and low potency. Fmoc-Cha-OH can be reversibly hydrolyzed to release free histidine, with a half life of around two hours. It binds to mitochondria, which are organelles found in cells that generate energy from food molecules. Fmoc-Cha-OH is an analog of the amino acid histidine, making it structurally similar but not identical.

Formula: C₂₄H₂₇NO₄

Purity: Min. 95%

Molecular weight: 393.49 g/mol

Ref: 3D-FLX-5545-PI