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2,3-Dichloro-DL-Phenylalanine is a chemical compound that is a derivative of phenylalanine, an essential amino acid involved in protein synthesis and various metabolic processes in the human body. The addition of dichloro groups to the phenylalanine molecule modifies its properties, potentially affecting its interactions with other molecules and its participation in biochemical reactions.

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  • 128833-94-3 Structure
  • Basic information

    1. Product Name: 2,3-Dichloro-DL-Phenylalanine
    2. Synonyms: 2,3-Dichloro-DL-Phenylalanine;H-DL-Phe(2,3-Cl2)-OH;2,3-Dichloro-DL-Phenylalanine hydrochloride
    3. CAS NO:128833-94-3
    4. Molecular Formula: C9H9Cl2NO2
    5. Molecular Weight: 234.07926
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 128833-94-3.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: 2,3-Dichloro-DL-Phenylalanine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3-Dichloro-DL-Phenylalanine(128833-94-3)
    11. EPA Substance Registry System: 2,3-Dichloro-DL-Phenylalanine(128833-94-3)
  • 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: 128833-94-3(Hazardous Substances Data)

128833-94-3 Usage

Uses

Used in Pharmaceutical Industry:
2,3-Dichloro-DL-Phenylalanine is used as a research compound for investigating its potential applications in drug development. Its unique properties, resulting from the dichloro modification, may offer new avenues for the treatment of various diseases and conditions.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2,3-Dichloro-DL-Phenylalanine serves as a valuable tool for studying the structure-activity relationships of phenylalanine-containing compounds. This can lead to the design of more effective drugs and therapeutic agents.
Used in Industrial Processes:
2,3-Dichloro-DL-Phenylalanine may also find applications in various industrial processes, where its altered properties can be utilized for specific purposes. However, further research is necessary to fully explore and understand its potential uses in these areas.

Check Digit Verification of cas no

The CAS Registry Mumber 128833-94-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,8,3 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 128833-94:
(8*1)+(7*2)+(6*8)+(5*8)+(4*3)+(3*3)+(2*9)+(1*4)=153
153 % 10 = 3
So 128833-94-3 is a valid CAS Registry Number.

128833-94-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-Dichlorophenylalanine

1.2 Other means of identification

Product number -
Other names 2-amino-3-(2,3-dichlorophenyl)propanoic acid

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:128833-94-3 SDS

128833-94-3Downstream Products

128833-94-3Relevant articles and documents

Synthesis and antitumor activity of platinum(II) complexes containing substituted ethylenediamine ligands

Brunner, Henri,Hankofer, Peter,Holzinger, Ulrich,Treittinger, Barbara,Schoenenberger, Helmut

, p. 35 - 44 (2007/10/02)

The synthesis of substituted ethylenediamines, their reactions with K2PtCl4 to give the dichloroplatinum(II) complexes, and the exchange of the chloro ligands for other leaving groups are described.The new compounds have been tested as antitumor agents both in vitro using the hormone independent human mammary carcinoma cell line MDA-MB 231 as well as in vivo using the lymphocytic P388 leukemia of the CD2F1-mouse.In the P388 test, 53 of the 55 tested complexes fulfill the minimum activity of 125percent T/C required for a substance to be active.

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