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CAS

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894413-41-3

BOC-DL-4-Acetylphenylalanine is a chemical compound that belongs to the class of acetylphenylalanine derivatives. It is characterized by a BOC (tert-butyloxycarbonyl) protecting group attached to the amino group of phenylalanine, and an acetyl group attached to the alpha amino group. BOC-DL-4-ACETYLPHENYLALANINE is commonly utilized in the field of organic chemistry and biochemistry for the production of novel peptide-based therapeutics and research purposes.

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  • 894413-41-3 Structure

  • Basic information

    1. Product Name: BOC-DL-4-ACETYLPHENYLALANINE
    2. Synonyms: BOC-DL-4-ACETYLPHENYLALANINE;Boc-4-Acetyl-DL-phenylalanine
    3. CAS NO:894413-41-3
    4. Molecular Formula: C16H21NO5
    5. Molecular Weight: 307.34
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 894413-41-3.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-DL-4-ACETYLPHENYLALANINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: BOC-DL-4-ACETYLPHENYLALANINE(894413-41-3)
    11. EPA Substance Registry System: BOC-DL-4-ACETYLPHENYLALANINE(894413-41-3)

  • 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: 894413-41-3(Hazardous Substances Data)

894413-41-3 Usage

Uses

Used in Pharmaceutical Industry:
BOC-DL-4-Acetylphenylalanine is used as a building block for the synthesis of peptides and pharmaceutical compounds. Its unique structure allows for the creation of novel peptide-based therapeutics with potential applications in various medical fields.
Used in Organic Chemistry Research:
BOC-DL-4-Acetylphenylalanine is employed as a research compound in organic chemistry. Its properties and reactivity can be studied to gain insights into the synthesis and modification of other acetylphenylalanine derivatives and related compounds.
Used in Biochemistry Research:
In biochemistry, BOC-DL-4-Acetylphenylalanine serves as a valuable research tool. It can be used to investigate the interactions between peptides and biological systems, as well as to explore the potential therapeutic effects of peptide-based compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 894413-41-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,4,4,1 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 894413-41:
(8*8)+(7*9)+(6*4)+(5*4)+(4*1)+(3*3)+(2*4)+(1*1)=193
193 % 10 = 3
So 894413-41-3 is a valid CAS Registry Number.

894413-41-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Phenylalanine, 4-acetyl-N-[(1,1-dimethylethoxy)carbonyl]-

1.2 Other means of identification

Product number -
Other names Boc-4-Acetyl-DL-phenylalanine

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:894413-41-3 SDS

894413-41-3Downstream Products

894413-41-3Relevant articles and documents

COMPOSITIONS CONTAINING, METHODS INVOLVING, AND USES OF NON-NATURAL AMINO ACIDS AND POLYPEPTIDES

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Paragraph 0545, (2016/07/27)

Disclosed herein are non-natural amino acids and polypeptides that include at least one non-natural amino acid, and methods for making such non-natural amino acids and polypeptides. The non-natural amino acids, by themselves or as a part of a polypeptide, can include a wide range of possible functionalities, but typical have at least one oxime, carbonyl, dicarbonyl, and/or hydroxylamine group. Also disclosed herein are non-natural amino acid polypeptides that are further modified post-translationally, methods for effecting such modifications, and methods for purifying such polypeptides. Typically, the modified non-natural amino acid polypeptides include at least one oximine, carbonyl, dicarbonyl, and/or hydroxylamine group. Further disclosed are methods for using such non-natural amino acid polypeptides and modified non-natural amino acid polypeptides, including therapeutic, diagnostic, and other biotechnology uses.

METHODS AND COMPOSITIONS FOR RIBOSOMAL SYNTHESIS OF MACROCYCLIC PEPTIDES

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Paragraph 00207, (2015/12/08)

Methods and compositions are provided for generating macrocyclic peptides from genetically encoded, ribosomally produced polypeptide precursors. Also provided are nucleic acid molecules, polypeptides, and methods for generating combinatorial libraries of

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