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3,4-Dichloro-L-Phenylalanine Methyl ester is a chemical compound with the molecular formula C11H12Cl2NO2. It is a derivative of the amino acid phenylalanine, featuring two chlorine atoms attached to the 3 and 4 positions of the phenyl ring and a methyl ester group at the carboxyl end. 3,4-Dichloro-L-Phenylalanine Methyl ester has been studied for its potential biological activity, particularly as a potential anticancer agent, and is often utilized as a building block in the synthesis of various pharmaceutical compounds and drug candidates. It is a valuable chemical with diverse applications in the fields of medicine and research.

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  • 173522-95-7 Structure
  • Basic information

    1. Product Name: 3,4-Dichloro-L-Phenylalanine Methyl ester
    2. Synonyms: 3,4-Dichloro-L-Phenylalanine Methyl ester;3,4-Dichloro-L-phenylalanine methyl ester hydrochloride
    3. CAS NO:173522-95-7
    4. Molecular Formula: C10H11Cl2NO2*ClH
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 173522-95-7.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.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 3,4-Dichloro-L-Phenylalanine Methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4-Dichloro-L-Phenylalanine Methyl ester(173522-95-7)
    11. EPA Substance Registry System: 3,4-Dichloro-L-Phenylalanine Methyl ester(173522-95-7)
  • 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: 173522-95-7(Hazardous Substances Data)

173522-95-7 Usage

Uses

Used in Pharmaceutical Industry:
3,4-Dichloro-L-Phenylalanine Methyl ester is used as a building block for the synthesis of pharmaceutical compounds and drug candidates. Its unique structure and functional groups make it a versatile component in the development of new medications.
Used in Research Applications:
3,4-Dichloro-L-Phenylalanine Methyl ester is used as a research tool to study its potential biological activity. It has been investigated for its possible anticancer properties, providing insights into the development of new cancer therapies.
Used in Anticancer Applications:
3,4-Dichloro-L-Phenylalanine Methyl ester is used as a potential anticancer agent. Its biological activity has been studied, and it may contribute to the development of new cancer treatments by targeting specific pathways or mechanisms involved in cancer progression.
Overall, 3,4-Dichloro-L-Phenylalanine Methyl ester is a multifaceted chemical compound with significant applications in the pharmaceutical and research sectors, particularly in the development of new drugs and therapies for various diseases, including cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 173522-95-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,5,2 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 173522-95:
(8*1)+(7*7)+(6*3)+(5*5)+(4*2)+(3*2)+(2*9)+(1*5)=137
137 % 10 = 7
So 173522-95-7 is a valid CAS Registry Number.

173522-95-7SDS

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 methyl (2S)-2-amino-3-(3,4-dichlorophenyl)propanoate

1.2 Other means of identification

Product number -
Other names 3,4-Dichloro-L-Phenylalanine Methyl ester

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:173522-95-7 SDS

173522-95-7Downstream Products

173522-95-7Relevant articles and documents

Rhodium-Catalyzed Enantioselective Synthesis of Oxazinones via an Asymmetric Ring Opening-Lactonization Cascade of Oxabicyclic Alkenes

Yen, Andy,Pham, Anh Hoang,Larin, Egor M.,Lautens, Mark

supporting information, p. 7549 - 7553 (2019/10/02)

The rhodium-catalyzed asymmetric ring opening reaction of oxabicyclic alkenes is shown to be an efficient method for synthesizing chiral heterocycles. We demonstrate that the pairwise combination of chiral catalyst with chiral amino-acid-derived pronucleophiles results in a stereodivergent synthesis of diastereomeric hydroxyesters. A favorable conformational preference induces the subsequent lactonization of one diastereomer leading to the highly enantioselective synthesis of oxazinones.

SULFONAMIDE COMPOUNDS

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Page/Page column 18, (2010/10/20)

Certain sulfonamide compounds are dual CCK1/CCK2 inhibitors useful in the treatment of CCK1/CCK2 mediated diseases.

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