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(S)-4-(1-AMINOETHYL)BENZOIC ACID, an organic compound with the molecular formula C9H11NO2 and a molecular weight of 165.19 g/mol, is a derivative of the amino acid phenylalanine. (S)-4-(1-AMINOETHYL)BENZOIC ACID features a unique structure with an additional amino group attached to the carbon atom of the benzene ring through a two-carbon linker. It is of significant interest in pharmaceutical research and drug development, particularly in the field of neuropharmacology, due to its potential as a neurotransmitter precursor and modulator. Furthermore, it may also serve as a building block for the synthesis of various bioactive compounds.

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  • 222714-33-2 Structure
  • Basic information

    1. Product Name: (S)-4-(1-AMINOETHYL)BENZOIC ACID
    2. Synonyms: 4-[(1S)-1-AMINOETHYL]-BENZOIC ACID;(S)-4-(1-AMINOETHYL)BENZOIC ACID;Benzoic acid, 4-[(1S)-1-aminoethyl]-;4-[(1S)-1-aMinoethyl]-;(S)-4-(1-aminoethyl)benzoic acid HCl
    3. CAS NO:222714-33-2
    4. Molecular Formula: C9H11NO2
    5. Molecular Weight: 165.19
    6. EINECS: N/A
    7. Product Categories: API intermediates
    8. Mol File: 222714-33-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 317°C at 760 mmHg
    3. Flash Point: 145.5°C
    4. Appearance: /
    5. Density: 1.186g/cm3
    6. Vapor Pressure: 0.000166mmHg at 25°C
    7. Refractive Index: 1.579
    8. Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
    9. Solubility: N/A
    10. PKA: 4.02±0.10(Predicted)
    11. CAS DataBase Reference: (S)-4-(1-AMINOETHYL)BENZOIC ACID(CAS DataBase Reference)
    12. NIST Chemistry Reference: (S)-4-(1-AMINOETHYL)BENZOIC ACID(222714-33-2)
    13. EPA Substance Registry System: (S)-4-(1-AMINOETHYL)BENZOIC ACID(222714-33-2)
  • 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: 222714-33-2(Hazardous Substances Data)

222714-33-2 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
(S)-4-(1-AMINOETHYL)BENZOIC ACID is used as a neurotransmitter precursor and modulator in the field of neuropharmacology for its potential therapeutic applications. It plays a crucial role in the regulation of neurotransmission, which can be beneficial in the treatment of various neurological disorders.
Used in the Synthesis of Bioactive Compounds:
(S)-4-(1-AMINOETHYL)BENZOIC ACID is used as a building block in the synthesis of various bioactive compounds. Its unique structure allows for the development of new pharmaceutical agents with potential applications in different therapeutic areas.
Used in Neuropharmacology:
In the field of neuropharmacology, (S)-4-(1-AMINOETHYL)BENZOIC ACID is used as a research compound to study the mechanisms of neurotransmission and develop new drugs targeting specific neurological pathways. Its ability to act as a neurotransmitter precursor and modulator makes it a valuable tool in understanding and treating neurological disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 222714-33-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,2,7,1 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 222714-33:
(8*2)+(7*2)+(6*2)+(5*7)+(4*1)+(3*4)+(2*3)+(1*3)=102
102 % 10 = 2
So 222714-33-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO2/c1-6(10)7-2-4-8(5-3-7)9(11)12/h2-6H,10H2,1H3,(H,11,12)/t6-/m0/s1

222714-33-2Upstream product

222714-33-2Relevant articles and documents

Piperazine compounds and medicinal use thereof

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, (2008/06/13)

The present invention relates to a piperazine compound of the formula wherein R1and R2are each hydrogen, halogen, lower alkyl, lower alkoxy, amino, substituted amino, nitro, hydroxy or cyano, R3, R4and R5are each hydrogen, halogen, lower alkyl, lower alkoxy, nitro, amino, substituted amino or hydroxy, R6and R7are each hydrogen, lower alkyl, lower alkyl substituted by halogen, aralkyl, acyl or lower acyl substituted by halogen, R8and R9are each hydrogen or lower alkyl, Y is lower alkylene and the like, and ring A is phenyl, pyrimidyl, thiazolyl, pyridyl, pyrazyl or imidazolyl, a pharmaceutically acceptable salt thereof and pharmaceutical agents containing these compounds. The compound of the present invention has superior TNF-α production inhibitory effect and/or IL-10 production promoting effect, and, since it is free of or shows only strikingly reduced expression of an effect on the central nervous system, the compound is useful as a highly safe and superior TNF-α production inhibitor an/or IL-10 production promoter and is useful as an agent for the prophylaxis or treatment of various diseases caused by abnormal TNF-α production, diseases curable with IL-10, such as chronic inflammatory diseases, acute inflammatory diseases, inflammatory diseases due to infection, autoimmune diseases, allergic diseases, and TNF-α mediated diseases.

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