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54143-11-2

3-Cyclopentene-1-carboxylic acid, 3-phenyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 54143-11-2 Structure

  • Basic information

    1. Product Name: 3-Cyclopentene-1-carboxylic acid, 3-phenyl- (9CI)
    2. Synonyms: 3-Cyclopentene-1-carboxylic acid, 3-phenyl- (9CI)
    3. CAS NO:54143-11-2
    4. Molecular Formula: C12H12O2
    5. Molecular Weight: 188.22248
    6. EINECS: N/A
    7. Product Categories: ACIDHALIDE
    8. Mol File: 54143-11-2.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: 3-Cyclopentene-1-carboxylic acid, 3-phenyl- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Cyclopentene-1-carboxylic acid, 3-phenyl- (9CI)(54143-11-2)
    11. EPA Substance Registry System: 3-Cyclopentene-1-carboxylic acid, 3-phenyl- (9CI)(54143-11-2)

  • 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: 54143-11-2(Hazardous Substances Data)

54143-11-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54143-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,4 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 54143-11:
(7*5)+(6*4)+(5*1)+(4*4)+(3*3)+(2*1)+(1*1)=92
92 % 10 = 2
So 54143-11-2 is a valid CAS Registry Number.

54143-11-2Relevant articles and documents

Mechanism-Based Design of an Amide-Directed Ni-Catalyzed Arylboration of Cyclopentene Derivatives

Lambright, Alison L.,Liu, Yanyao,Joyner, Isaac A.,Logan, Kaitlyn M.,Brown, M. Kevin

, p. 612 - 616 (2021/01/26)

A method for amide-directed Ni-catalyzed diastereoselective arylboration of cyclopentenes is disclosed. The reaction allows for the synthesis of sterically congested cyclopentane scaffolds that contain an easily derivatized boronic ester and amide functional handles. The nature of the amide directing group and its influence on the reaction outcome are investigated and ultimately reflect a predictably selective reaction based on the solvent and base counterion.

1,3-SUBSTITUTED CYCLOALKENES AND CYCLOALKANES AS CENTRAL NERVOUS SYSTEM AGENTS

-

, (2008/06/13)

1,3-Substituted cycloalkenes and cycloalkanes are described, as well as methods for the preparation and pharmaceutical composition of same, which are useful as central nervous system agents and are particularly useful as dopaminergic, antipsychotic, and a

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