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261380-34-1

Boc-(R)-2-aMino-3-(4-ethylphenyl)propanoic acid is a chiral amino acid derivative with the molecular formula C15H23NO4. It features a Boc (t-butoxycarbonyl) protecting group and has a specific (R)-configuration, which gives it a unique spatial arrangement of atoms. Boc-(R)-2-aMino-3-(4-ethylphenyl)propanoic acid is commonly utilized in organic synthesis and peptide chemistry as a key building block for the preparation of peptides and other bioactive molecules.

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  • 261380-34-1 Structure

  • Basic information

    1. Product Name: Boc-(R)-2-aMino-3-(4-ethylphenyl)propanoic acid
    2. Synonyms: Boc-(R)-2-aMino-3-(4-ethylphenyl)propanoic acid;N-Boc-4-ethyl-D-phenylalanine
    3. CAS NO:261380-34-1
    4. Molecular Formula: C16H23NO4
    5. Molecular Weight: 293.35812
    6. EINECS: N/A
    7. Product Categories: unnatural amino acids
    8. Mol File: 261380-34-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Boc-(R)-2-aMino-3-(4-ethylphenyl)propanoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: Boc-(R)-2-aMino-3-(4-ethylphenyl)propanoic acid(261380-34-1)
    11. EPA Substance Registry System: Boc-(R)-2-aMino-3-(4-ethylphenyl)propanoic acid(261380-34-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 261380-34-1(Hazardous Substances Data)

261380-34-1 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
Boc-(R)-2-aMino-3-(4-ethylphenyl)propanoic acid serves as an essential component in the synthesis of complex peptide-based therapeutics. Its role in creating bioactive molecules makes it a valuable asset in the development of new pharmaceuticals.
Used in Organic Synthesis:
As a building block in organic synthesis, Boc-(R)-2-aMino-3-(4-ethylphenyl)propanoic acid contributes to the creation of a wide range of chemical compounds, expanding the possibilities for various applications across different industries.
Used in Peptide Chemistry:
In peptide chemistry, Boc-(R)-2-aMino-3-(4-ethylphenyl)propanoic acid is a crucial constituent for the assembly of peptides. Its presence allows for the development of peptide-based drugs and other biologically active substances.

Check Digit Verification of cas no

The CAS Registry Mumber 261380-34-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,1,3,8 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 261380-34:
(8*2)+(7*6)+(6*1)+(5*3)+(4*8)+(3*0)+(2*3)+(1*4)=121
121 % 10 = 1
So 261380-34-1 is a valid CAS Registry Number.

261380-34-1Downstream Products

261380-34-1Relevant articles and documents

BENZIMIDAZOLYL-METHYL UREA DERIVATIVES AS ALX RECEPTOR AGONISTS

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Page/Page column 92; 155, (2015/02/25)

The present invention relates to benzimidazolyl-methyl urea derivatives of formula (I), wherein n, D, E, R1, R2, R3, R4, R6, R7, R8 and R9 are as defined in the description, their preparation and their use as pharmaceutically active compounds.

THE ANALOGS OF 8-D-HOMOARGININE-VASOPRESSIN WITH p-SUBSTITUTED PHENYLALANINE IN POSITION 2; SYNTHESIS AND SOME BIOLOGICAL PROPERTIES

Zertova, Miroslava,Prochazka, Zdenko,Blaha, Ivo,Barth, Tomislav,Slaninova, Jirina,et al.

, p. 3000 - 3007 (2007/10/02)

Solid phase methodology on benzhydrylamine resin was used for the synthesis of five analogs of vasopressin with no-coded amino acid, D-homoarginine, in position 8 and p-substituted D or L phenylalanine in position 2.Besides the mother analog, 8

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