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FMOC-(S)-3-AMINO-3-(3-CHLORO-PHENYL)-PROPIONIC ACID is a chemical compound utilized in organic chemistry, characterized by the attachment of a fluorophenylmethyloxycarbonyl (FMOC) protecting group to the molecule of (S)-3-amino-3-(3-chlorophenyl)-propionic acid. FMOC-(S)-3-AMINO-3-(3-CHLORO-PHENYL)-PROPIONIC ACID is distinguished by its ability to serve as a starting material for peptide synthesis and the creation of other organic molecules, facilitated by the FMOC group's easy removal under mild conditions, thereby revealing the free amine group. The incorporation of an amino acid and a chlorophenyl group endows it with potential as a building block in the design and synthesis of innovative pharmaceutical compounds.

507472-16-4

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507472-16-4 Usage

Uses

Used in Pharmaceutical Synthesis:
FMOC-(S)-3-AMINO-3-(3-CHLORO-PHENYL)-PROPIONIC ACID is used as a building block for the development of novel pharmaceutical compounds, leveraging its structural components to create new drug candidates with potential therapeutic applications.
Used in Peptide Synthesis:
In the field of peptide synthesis, FMOC-(S)-3-AMINO-3-(3-CHLORO-PHENYL)-PROPIONIC ACID is utilized as a starting material. The FMOC group's ease of removal under mild conditions allows for the controlled assembly of peptide chains, facilitating the synthesis of complex peptide structures.
Used in Organic Chemistry Research:
FMOC-(S)-3-AMINO-3-(3-CHLORO-PHENYL)-PROPIONIC ACID is employed as a research tool in organic chemistry, providing insights into the reactivity and properties of molecules containing both FMOC protecting groups and functional groups like amino acids and chlorophenyl moieties.
Used in Chemical Education:
FMOC-(S)-3-AMINO-3-(3-CHLORO-PHENYL)-PROPIONIC ACID can also be used in educational settings to illustrate the principles of protecting group chemistry and the synthesis of complex organic molecules, offering a practical example for students to understand the concepts of organic synthesis and the role of protecting groups in facilitating the formation of desired products.

Check Digit Verification of cas no

The CAS Registry Mumber 507472-16-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,7,4,7 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 507472-16:
(8*5)+(7*0)+(6*7)+(5*4)+(4*7)+(3*2)+(2*1)+(1*6)=144
144 % 10 = 4
So 507472-16-4 is a valid CAS Registry Number.
InChI:InChI=1/C24H20ClNO4/c25-16-7-5-6-15(12-16)22(13-23(27)28)26-24(29)30-14-21-19-10-3-1-8-17(19)18-9-2-4-11-20(18)21/h1-12,21-22H,13-14H2,(H,26,29)(H,27,28)/t22-/m0/s1

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