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(S)-FMOC-4-TERT-BUTYLTHIOPHENYLALANINE is a chemical compound and an amino acid derivative of phenylalanine, featuring a tert-butylthio group attached to its phenyl ring. (S)-FMOC-4-TERT-BUTYLTHIOPHENYLALANINE is equipped with an FMOC (9-fluorenylmethoxycarbonyl) protecting group, which renders it highly suitable for solid-phase peptide synthesis, a prevalent technique in the creation of peptides for research and medicinal applications.

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  • L-Phenylalanine,4-[(1,1-dimethylethyl)thio]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-

    Cas No: 204716-12-1

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  • 204716-12-1 Structure
  • Basic information

    1. Product Name: (S)-FMOC-4-TERT-BUTYLTHIOPHENYLALANINE
    2. Synonyms: FMOC-L-PHE(4-S-TBU);FMOC-D, L-PHE(4-S-TBU);FMOC-S-PHE(4-STBU)-OH;(S)-N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-4-T-BUTYLTHIO-PHENYLALANINE;(S)-FMOC-4-TERT-BUTYLTHIOPHENYLALANINE;(S)-N-alpha-(9-Fluoromethyloxycarbonyl)-4-t-butylthio-phenylalanine
    3. CAS NO:204716-12-1
    4. Molecular Formula: C28H29NO4S
    5. Molecular Weight: 475.6
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 204716-12-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 677.0±55.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.27±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 3.76±0.10(Predicted)
    10. CAS DataBase Reference: (S)-FMOC-4-TERT-BUTYLTHIOPHENYLALANINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: (S)-FMOC-4-TERT-BUTYLTHIOPHENYLALANINE(204716-12-1)
    12. EPA Substance Registry System: (S)-FMOC-4-TERT-BUTYLTHIOPHENYLALANINE(204716-12-1)
  • 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: 204716-12-1(Hazardous Substances Data)

204716-12-1 Usage

Uses

Used in Pharmaceutical Industry:
(S)-FMOC-4-TERT-BUTYLTHIOPHENYLALANINE is utilized as a building block in peptide synthesis for the development of peptide-based drugs. Its unique structure and the presence of the FMOC protecting group facilitate the synthesis process, allowing for the creation of complex peptide sequences with potential therapeutic applications.
Used in Biotechnology Industry:
In the biotechnology sector, (S)-FMOC-4-TERT-BUTYLTHIOPHENYLALANINE serves as a crucial component in the production of research tools. Its incorporation into peptides can lead to the discovery of new bioactive molecules with specific functions, contributing to advancements in various areas of biological research.
Additionally, due to its potential pharmacological properties, (S)-FMOC-4-TERT-BUTYLTHIOPHENYLALANINE is under investigation for its possible applications in drug discovery, where it could contribute to the development of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 204716-12-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,7,1 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 204716-12:
(8*2)+(7*0)+(6*4)+(5*7)+(4*1)+(3*6)+(2*1)+(1*2)=101
101 % 10 = 1
So 204716-12-1 is a valid CAS Registry Number.

204716-12-1SDS

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)-3-(4-tert-butylphenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanethioic S-acid

1.2 Other means of identification

Product number -
Other names CTK4E4312

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:204716-12-1 SDS

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