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FMOC-MENVA-OH is a chemical compound frequently utilized in scientific research, particularly in the fields of chemistry and biochemistry. It is specifically designed for use in peptide synthesis, a process that forms peptide bonds to create unique peptides. The "FMOC" or 9-fluorenylmethoxy carbonyl group in FMOC-MENVA-OH serves as a protective agent for the amine group during peptide synthesis. The "MENVA" in its name indicates the specific sequence of amino acids that this compound is intended to produce. FMOC-MENVA-OH is primarily used in laboratory settings and is not intended for consumption or applications outside of research purposes.

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  • 252049-05-1 Structure
  • Basic information

    1. Product Name: FMOC-MENVA-OH
    2. Synonyms: N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-ALPHA-METHYL-L-NORVALINE;N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-N-ALPHA-METHYL-NORVALINE;N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-N-ALPHA-METHYL-L-NORVALINE;N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-N-ALPHA-METHYL-L-2-AMINOPENTANOIC ACID;N-ALPHA-FMOC-N-ALPHA-METHYL-L-NORVALINE;FMOC-L-MENCH[CH3(CH2)2]-COOH;FMOC-L-MENVA-OH;FMOC-L-N-METHYL-2-AMINOVALERIC ACID
    3. CAS NO:252049-05-1
    4. Molecular Formula: C21H23NO4
    5. Molecular Weight: 353.41
    6. EINECS: N/A
    7. Product Categories: amino acids
    8. Mol File: 252049-05-1.mol
  • Chemical Properties

    1. Melting Point: 130.0 to 135.0 °C
    2. Boiling Point: 533.1±29.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /Solid
    5. Density: 1 +-.0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Store at RT.
    8. Solubility: N/A
    9. PKA: 3.92±0.20(Predicted)
    10. CAS DataBase Reference: FMOC-MENVA-OH(CAS DataBase Reference)
    11. NIST Chemistry Reference: FMOC-MENVA-OH(252049-05-1)
    12. EPA Substance Registry System: FMOC-MENVA-OH(252049-05-1)
  • 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: 252049-05-1(Hazardous Substances Data)

252049-05-1 Usage

Uses

Used in Peptide Synthesis:
FMOC-MENVA-OH is used as a building block in the synthesis of peptides for [application reason], contributing to the formation of specific peptide sequences. The FMOC group provides protection for the amine group, ensuring that the peptide synthesis process proceeds accurately and efficiently.
Used in Scientific Research:
FMOC-MENVA-OH is used as a research tool in [application reason], allowing scientists to explore the properties and potential applications of newly synthesized peptides. Its role in peptide synthesis makes it a valuable asset in the development of new drugs, vaccines, and other bioactive molecules.
Used in Chemistry and Biochemistry:
FMOC-MENVA-OH is used as a reagent in [application reason], facilitating the study of peptide chemistry and the interactions between amino acids. Its presence in the laboratory helps researchers understand the fundamental principles of peptide bond formation and the factors that influence the stability and functionality of peptides.
Used in Drug Development:
FMOC-MENVA-OH is used as a component in the development of new pharmaceuticals for [application reason], as it enables the synthesis of peptides with potential therapeutic properties. The ability to create specific peptide sequences using FMOC-MENVA-OH can lead to the discovery of novel drugs with improved efficacy and reduced side effects.
Used in Vaccine Production:
FMOC-MENVA-OH is used in the production of vaccines for [application reason], as it can be used to synthesize peptide-based vaccines. These vaccines can be designed to target specific pathogens, providing a more targeted and effective approach to immunization.
Used in Biochemical Analysis:
FMOC-MENVA-OH is used as an analytical tool in [application reason], allowing researchers to study the structure and function of peptides at the molecular level. Its role in peptide synthesis can help scientists gain insights into the mechanisms of protein folding, enzyme activity, and other biochemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 252049-05-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,2,0,4 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 252049-05:
(8*2)+(7*5)+(6*2)+(5*0)+(4*4)+(3*9)+(2*0)+(1*5)=111
111 % 10 = 1
So 252049-05-1 is a valid CAS Registry Number.

252049-05-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
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  • Alfa Aesar

  • (H63454)  N-Fmoc-N-methyl-L-norvaline, 95%   

  • 252049-05-1

  • 250mg

  • 753.0CNY

  • Detail
  • Alfa Aesar

  • (H63454)  N-Fmoc-N-methyl-L-norvaline, 95%   

  • 252049-05-1

  • 1g

  • 2254.0CNY

  • Detail
  • Alfa Aesar

  • (H63454)  N-Fmoc-N-methyl-L-norvaline, 95%   

  • 252049-05-1

  • 5g

  • 9036.0CNY

  • Detail

252049-05-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-[9H-fluoren-9-ylmethoxycarbonyl(methyl)amino]pentanoic acid

1.2 Other means of identification

Product number -
Other names (2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl](methyl)amino}pentanoic 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:252049-05-1 SDS

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