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Z-PHE-LEU-ALA-OH is a peptide consisting of the amino acids phenylalanine (Phe), leucine (Leu), and alanine (Ala), with a C-terminal hydroxyl group (OH). This specific sequence of amino acids endows Z-PHE-LEU-ALA-OH with unique physical and chemical properties, making it a subject of interest for its potential biological activities, enzymatic substrate roles, and interactions with other molecules in the body. Its potential therapeutic applications as a drug or a research tool in biochemistry and pharmacology are currently under investigation.

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  • L-Alanine,N-[(phenylmethoxy)carbonyl]-L-phenylalanyl-L-leucyl- (9CI)

    Cas No: 24955-29-1

  • USD $ 1.9-2.9 / Gram

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  • 24955-29-1 Structure
  • Basic information

    1. Product Name: Z-PHE-LEU-ALA-OH
    2. Synonyms: CBZ-PHE-LEU-ALA;Z-PHE-LEU-ALA-OH
    3. CAS NO:24955-29-1
    4. Molecular Formula: C26H33N3O6
    5. Molecular Weight: 483.56
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 24955-29-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 785.9°Cat760mmHg
    3. Flash Point: 429.1°C
    4. Appearance: /
    5. Density: 1.204g/cm3
    6. Vapor Pressure: 5.09E-26mmHg at 25°C
    7. Refractive Index: 1.56
    8. Storage Temp.: -15°C
    9. Solubility: N/A
    10. CAS DataBase Reference: Z-PHE-LEU-ALA-OH(CAS DataBase Reference)
    11. NIST Chemistry Reference: Z-PHE-LEU-ALA-OH(24955-29-1)
    12. EPA Substance Registry System: Z-PHE-LEU-ALA-OH(24955-29-1)
  • 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: 24955-29-1(Hazardous Substances Data)

24955-29-1 Usage

Uses

Used in Pharmaceutical Research:
Z-PHE-LEU-ALA-OH is used as a substrate in enzymatic reactions for studying the mechanisms of enzyme action and the development of new drugs targeting specific enzymes.
Used in Biochemical Research:
Z-PHE-LEU-ALA-OH is used as a research tool to investigate the interactions between peptides and other molecules, such as receptors or enzymes, to better understand the underlying processes in biological systems.
Used in Drug Development:
Z-PHE-LEU-ALA-OH is used as a potential therapeutic agent in the development of new drugs, given its unique properties and potential biological activities. Further research is required to explore its full potential and establish its efficacy and safety in various therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 24955-29-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,9,5 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24955-29:
(7*2)+(6*4)+(5*9)+(4*5)+(3*5)+(2*2)+(1*9)=131
131 % 10 = 1
So 24955-29-1 is a valid CAS Registry Number.
InChI:InChI=1/C26H33N3O6/c1-17(2)14-21(23(30)27-18(3)25(32)33)28-24(31)22(15-19-10-6-4-7-11-19)29-26(34)35-16-20-12-8-5-9-13-20/h4-13,17-18,21-22H,14-16H2,1-3H3,(H,27,30)(H,28,31)(H,29,34)(H,32,33)

24955-29-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[4-methyl-2-[[3-phenyl-2-(phenylmethoxycarbonylamino)propanoyl]amino]pentanoyl]amino]propanoic acid

1.2 Other means of identification

Product number -
Other names Cbz-Phe-Leu-Ala-OH

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:24955-29-1 SDS

24955-29-1Upstream product

24955-29-1Relevant articles and documents

Fully enzymatic peptide synthesis using C-terminal tert-butyl ester interconversion

Nuijens, Timo,Cusan, Claudia,Van Dooren, Theodorus J. G. M.,Moody, Harold M.,Merkx, Remco,Kruijtzer, John A. W.,Rijkers, Dirk T. S.,Liskamp, Rob M. J.,Quaedflieg, Peter J. L. M.

experimental part, p. 2399 - 2404 (2011/02/21)

Chemoenzymatic peptide synthesis is potentially the most cost-efficient technology for the synthesis of short and medium-sized peptides with some important advantages. For instance, stoichiometric amounts of expensive coupling reagents are not required an

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