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209224-98-6

2,3-Dihydro-1H-cyclopenta[a]naphthalene-2-carboxylic acid is a carboxylic acid derivative of naphthalene with the molecular formula C15H12O2. It is a chemical compound that serves as a starting material for the synthesis of various pharmaceuticals and organic compounds. Its unique chemical structure and properties have been studied for their potential anti-inflammatory and analgesic properties, making it a promising candidate for drug development and treatment of medical conditions such as arthritis and cancer.

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  • 209224-98-6 Structure

  • Basic information

    1. Product Name: 2,3-DIHYDRO-1H-CYCLOPENTA[A]NAPHTHALENE-2-CARBOXYLIC ACID
    2. Synonyms: 2,3-DIHYDRO-1H-CYCLOPENTA[A]NAPHTHALENE-2-CARBOXYLIC ACID
    3. CAS NO:209224-98-6
    4. Molecular Formula: C14H12O2
    5. Molecular Weight: 212.24388
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 209224-98-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 430.0±34.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.287±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 4.41±0.20(Predicted)
    10. CAS DataBase Reference: 2,3-DIHYDRO-1H-CYCLOPENTA[A]NAPHTHALENE-2-CARBOXYLIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,3-DIHYDRO-1H-CYCLOPENTA[A]NAPHTHALENE-2-CARBOXYLIC ACID(209224-98-6)
    12. EPA Substance Registry System: 2,3-DIHYDRO-1H-CYCLOPENTA[A]NAPHTHALENE-2-CARBOXYLIC ACID(209224-98-6)

  • 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: 209224-98-6(Hazardous Substances Data)

209224-98-6 Usage

Uses

Used in Pharmaceutical Industry:
2,3-Dihydro-1H-cyclopenta[a]naphthalene-2-carboxylic acid is used as a starting material for the synthesis of various pharmaceuticals and organic compounds. Its unique chemical structure and properties make it an important intermediate in organic synthesis and drug discovery research.
Used in Drug Development:
2,3-Dihydro-1H-cyclopenta[a]naphthalene-2-carboxylic acid is used as a potential candidate for drug development due to its potential anti-inflammatory and analgesic properties. It has been studied for its potential use in the treatment of various medical conditions, including arthritis and cancer.
Used in Organic Synthesis Research:
2,3-Dihydro-1H-cyclopenta[a]naphthalene-2-carboxylic acid is used as an important intermediate in organic synthesis research. Its unique chemical structure and properties make it a valuable compound for the development of new organic compounds and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 209224-98-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,2,2 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 209224-98:
(8*2)+(7*0)+(6*9)+(5*2)+(4*2)+(3*4)+(2*9)+(1*8)=126
126 % 10 = 6
So 209224-98-6 is a valid CAS Registry Number.

209224-98-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-DIHYDRO-1H-CYCLOPENTA[A]NAPHTHALENE-2-CARBOXYLIC ACID

1.2 Other means of identification

Product number -
Other names 4:5-Benzindan-2-carbonsaeure

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:209224-98-6 SDS

209224-98-6Downstream Products

209224-98-6Relevant articles and documents

Design and synthesis of the potent, orally available, brain-penetrable arylpyrazole class of neuropeptide Y5 receptor antagonists

Sato, Nagaaki,Takahashi, Toshiyuki,Shibata, Takunobu,Haga, Yuji,Sakuraba, Aya,Hirose, Masaaki,Sato, Miki,Nonoshita, Katsumasa,Koike, Yuko,Kitazawa, Hidefumi,Fujino, Naoko,Ishii, Yasuyuki,Ishihara, Akane,Kanatani, Akio,Fukami, Takehiro

, p. 666 - 669 (2007/10/03)

Novel arylpyrazole derivatives were synthesized and evaluated as neuropeptide Y (NPY) Y5 receptor antagonists. Compound (-)-7, which features a novel chiral 2,3-dihydro-1H-cyclopenta [a] naphthalene moiety, showed good binding affinity and antagonistic ac

Pyrazole derivatives

-

, (2008/06/13)

The present invention relates to a compound represented by the general formula [I]: wherein A and B rings are ortho-condensed to each other, A ring represents an aromatic carbocyclic or heterocyclic ring and B ring represents an aliphatic four- to seven-m

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