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FMOC-(S)-2-AMINO-3-METHOXYPROPIONIC ACID is a chemical compound that serves as a crucial component in the synthesis of peptides and peptidomimetics. It is a derivative of 2-amino-3-methoxypropionic acid, a nonproteinogenic amino acid, and is widely utilized in solid-phase peptide synthesis as a protecting group. The FMOC (9-fluorenylmethyloxycarbonyl) group attached to this compound is known for its ability to protect the amine group of amino acids during peptide synthesis, allowing for its easy removal under mild conditions. This makes FMOC-(S)-2-AMINO-3-METHOXYPROPIONIC ACID a significant player in the realm of medicinal chemistry and drug discovery, where it is instrumental in the creation of innovative peptide-based drugs and the study of peptide-protein interactions.

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    Cas No: 159610-93-2

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  • (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-methoxypropanoic acid

    Cas No: 159610-93-2

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  • 159610-93-2 Structure
  • Basic information

    1. Product Name: FMOC-(S)-2-AMINO-3-METHOXYPROPIONIC ACID
    2. Synonyms: N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-O-METHYL-L-SERINE;FMOC-L-SER(ME)-OH;FMOC-O-METHYL-L-SER;FMOC-(S)-2-AMINO-3-METHOXYLPROPANOIC ACID;FMOC-(S)-2-AMINO-3-METHOXYPROPIONIC ACID;FMoc-Ser(Me)-OH;N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-O-methyl-L-serine;(9H-Fluoren-9-yl)MethOxy]Carbonyl Ser(Me)-OH
    3. CAS NO:159610-93-2
    4. Molecular Formula: C19H19NO5
    5. Molecular Weight: 341.36
    6. EINECS: N/A
    7. Product Categories: unnatural amino acids
    8. Mol File: 159610-93-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 567.9±50.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.285±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: 3.41±0.10(Predicted)
    10. CAS DataBase Reference: FMOC-(S)-2-AMINO-3-METHOXYPROPIONIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: FMOC-(S)-2-AMINO-3-METHOXYPROPIONIC ACID(159610-93-2)
    12. EPA Substance Registry System: FMOC-(S)-2-AMINO-3-METHOXYPROPIONIC ACID(159610-93-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 159610-93-2(Hazardous Substances Data)

159610-93-2 Usage

Uses

Used in Pharmaceutical Industry:
FMOC-(S)-2-AMINO-3-METHOXYPROPIONIC ACID is used as a key intermediate in the synthesis of peptide-based drugs for its ability to facilitate the formation of complex peptide structures. Its role in protecting the amine group during synthesis ensures the integrity and functionality of the final drug product.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, FMOC-(S)-2-AMINO-3-METHOXYPROPIONIC ACID is used as a building block for the development of novel therapeutic agents. Its unique properties allow researchers to explore new avenues in drug design and the creation of compounds with specific biological activities.
Used in Peptide Synthesis:
FMOC-(S)-2-AMINO-3-METHOXYPROPIONIC ACID is used as a protecting group in solid-phase peptide synthesis to shield the amine group of amino acids. This protection is vital for preventing unwanted side reactions during the assembly of peptide chains, thereby enhancing the yield and purity of the final peptide product.
Used in Drug Discovery:
FMOC-(S)-2-AMINO-3-METHOXYPROPIONIC ACID is utilized in drug discovery processes to create and investigate peptide-protein interactions. Understanding these interactions is crucial for identifying potential drug targets and developing new therapeutic strategies to combat various diseases.
Overall, FMOC-(S)-2-AMINO-3-METHOXYPROPIONIC ACID is a versatile and essential compound in the fields of pharmaceuticals, medicinal chemistry, and drug discovery, playing a pivotal role in the advancement of peptide-based therapeutics and our understanding of biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 159610-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,6,1 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 159610-93:
(8*1)+(7*5)+(6*9)+(5*6)+(4*1)+(3*0)+(2*9)+(1*3)=152
152 % 10 = 2
So 159610-93-2 is a valid CAS Registry Number.

159610-93-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-methoxypropanoic acid

1.2 Other means of identification

Product number -
Other names (2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-3-methoxypropanoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:159610-93-2 SDS

159610-93-2Downstream Products

159610-93-2Relevant articles and documents

Kras inhibitory cyclic peptide compound

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Paragraph 0362; 0481-0482, (2021/06/03)

The following were discovered: a cyclic peptide compound that interacts with Ras; and an unnatural amino acid that is useful in the production of said cyclic peptide compound. The cyclic peptide compound was also discovered to inhibit bonding between Ras and SOS. The following were additionally discovered: a specific unnatural amino acid included in said cyclic peptide compound; and a manufacturing method therefor.

Compounds for enzyme inhibition

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Page/Page column 33; 34, (2008/06/13)

Peptide-based compounds including heteroatom-containing, three-membered rings efficiently and selectively inhibit specific activities of N-terminal nucleophile (Ntn) hydrolases associated with the proteasome. The peptide-based compounds include an epoxide

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