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AMINO-(4-ETHYL-PHENYL)-ACETIC ACID, with the molecular formula C10H13NO2, is an amino acid derivative characterized by the presence of a phenyl group with an ethyl substitution at the para position. AMINO-(4-ETHYL-PHENYL)-ACETIC ACID is primarily utilized for research purposes, given its structural resemblance to other amino acids and phenylacetic acid derivatives, which may confer it with potential pharmaceutical or biological activities. However, its full potential uses and effects are yet to be comprehensively explored through further research and testing.

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  • 318270-08-5 Structure
  • Basic information

    1. Product Name: AMINO-(4-ETHYL-PHENYL)-ACETIC ACID
    2. Synonyms: 2-AMINO-2-(4-ETHYLPHENYL)ACETIC ACID;AMINO-(4-ETHYL-PHENYL)-ACETIC ACID
    3. CAS NO:318270-08-5
    4. Molecular Formula: C10H13NO2
    5. Molecular Weight: 179.22
    6. EINECS: N/A
    7. Product Categories: pharmacetical
    8. Mol File: 318270-08-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 321.3°C at 760 mmHg
    3. Flash Point: 148.1°C
    4. Appearance: /
    5. Density: 1.162g/cm3
    6. Vapor Pressure: 0.000125mmHg at 25°C
    7. Refractive Index: 1.568
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 2.02±0.10(Predicted)
    11. CAS DataBase Reference: AMINO-(4-ETHYL-PHENYL)-ACETIC ACID(CAS DataBase Reference)
    12. NIST Chemistry Reference: AMINO-(4-ETHYL-PHENYL)-ACETIC ACID(318270-08-5)
    13. EPA Substance Registry System: AMINO-(4-ETHYL-PHENYL)-ACETIC ACID(318270-08-5)
  • 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: 318270-08-5(Hazardous Substances Data)

318270-08-5 Usage

Uses

Used in Research Applications:
AMINO-(4-ETHYL-PHENYL)-ACETIC ACID is used as a research chemical for [application reason], given its unique structural properties that may offer insights into the development of new pharmaceuticals or biological agents. Its potential applications in this field are currently under investigation due to its structural similarity to other known active compounds.
Given the limited information on commercial applications, the specific uses in various industries are not detailed in the provided materials. Further research would be necessary to identify and validate its applications beyond the research context.

Check Digit Verification of cas no

The CAS Registry Mumber 318270-08-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,8,2,7 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 318270-08:
(8*3)+(7*1)+(6*8)+(5*2)+(4*7)+(3*0)+(2*0)+(1*8)=125
125 % 10 = 5
So 318270-08-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO2/c1-2-7-3-5-8(6-4-7)9(11)10(12)13/h3-6,9H,2,11H2,1H3,(H,12,13)

318270-08-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-2-(4-ethylphenyl)acetic acid

1.2 Other means of identification

Product number -
Other names AMINO-(4-ETHYL-PHENYL)-ACETIC 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:318270-08-5 SDS

318270-08-5Upstream product

318270-08-5Relevant articles and documents

Synthesis of new imidazolidin-2,4-dione and 2-thioxoimidazolidin-4-ones via C-phenylglycine derivatives

De Sousa Luis, Jose Alixandre,Barbosa Filho, Jose Maria,Lira, Bruno Freitas,Medeiros, Isac Almeida,De Morais, Liana Clebia Soares Lima,Dos Santos, Alexsandro Fernandes,De Oliveira, Cledualdo Soares,De Athayde-Filho, Petronio Filgueiras

experimental part, p. 128 - 137 (2010/05/18)

Hydantoins and their derivatives constitute a group of pharmaceutical compounds with anticonvulsant and antiarrhythmic properties, and are also used against diabetes. N-3 and C-5 substituted imidazolidines are examples of such products. As such, we have developed a synthesis of 2,4-dione and 2-thioxo-4-one imidazolidinic derivatives by reaction of amino acids with C-phenylglycine, phenyl isocyanate and phenyl isothiocyanate. Four amino-derivatives IG(1-4) and eight imidazolidinic derivatives, IM(1-8), were obtained in yields of 70-74%. The mass, infrared, 1H and 13C-NMR spectra of representative products are discussed.

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