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1195941-38-8

2-[4-methoxy-3-(2-m-tolyl-ethoxy)-benzoylamino]-indane-2-carboxylic acid is a complex organic compound characterized by an indane core structure, to which a benzoylamino group and a carboxylic acid group are attached. The benzoylamino group features a 4-methoxy-3-(2-m-tolyl-ethoxy) moiety, contributing to the compound's unique chemical properties. This intricate molecular architecture suggests potential applications in the pharmaceutical sector, particularly in the realm of drug development and therapeutic innovation.

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  • 1195941-38-8 Structure

  • Basic information

    1. Product Name: 2-[4-methoxy-3-(2-m-tolyl-ethoxy)-benzoylamino]-indane-2-carboxylic acid
    2. Synonyms: 2-[4-methoxy-3-(2-m-tolyl-ethoxy)-benzoylamino]-indane-2-carboxylic acid
    3. CAS NO:1195941-38-8
    4. Molecular Formula: C27H27NO5
    5. Molecular Weight: 445.515
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1195941-38-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 659.0±55.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: 1.28±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-[4-methoxy-3-(2-m-tolyl-ethoxy)-benzoylamino]-indane-2-carboxylic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[4-methoxy-3-(2-m-tolyl-ethoxy)-benzoylamino]-indane-2-carboxylic acid(1195941-38-8)
    11. EPA Substance Registry System: 2-[4-methoxy-3-(2-m-tolyl-ethoxy)-benzoylamino]-indane-2-carboxylic acid(1195941-38-8)

  • 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: 1195941-38-8(Hazardous Substances Data)

1195941-38-8 Usage

Uses

Used in Pharmaceutical Industry:
2-[4-methoxy-3-(2-m-tolyl-ethoxy)-benzoylamino]-indane-2-carboxylic acid is used as a potential drug candidate for the development of new therapeutic agents. Its unique structure and functional groups may offer novel mechanisms of action and selectivity profiles, which could be harnessed to address unmet medical needs or improve upon existing treatments.
Used in Drug Discovery:
In the field of drug discovery, 2-[4-methoxy-3-(2-m-tolyl-ethoxy)-benzoylamino]-indane-2-carboxylic acid serves as a starting point for the synthesis of new chemical entities. Its structural features may be modified or optimized to enhance pharmacokinetic properties, such as solubility, stability, and bioavailability, as well as to improve pharmacodynamic characteristics, including potency, selectivity, and safety.
Used in Medicinal Chemistry Research:
2-[4-methoxy-3-(2-m-tolyl-ethoxy)-benzoylamino]-indane-2-carboxylic acid is utilized as a research tool in medicinal chemistry to explore the structure-activity relationships (SAR) of related compounds. Understanding how variations in the chemical structure impact biological activity can guide the design of more effective and safer drugs.
Further research and testing are required to fully elucidate the properties and potential applications of 2-[4-methoxy-3-(2-m-tolyl-ethoxy)-benzoylamino]-indane-2-carboxylic acid, ensuring that its use in the pharmaceutical industry is grounded in scientific evidence and aligned with regulatory standards.

Check Digit Verification of cas no

The CAS Registry Mumber 1195941-38-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,5,9,4 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1195941-38:
(9*1)+(8*1)+(7*9)+(6*5)+(5*9)+(4*4)+(3*1)+(2*3)+(1*8)=188
188 % 10 = 8
So 1195941-38-8 is a valid CAS Registry Number.

1195941-38-8Relevant articles and documents

ACYLAMINO-SUBSTITUTED FUSED CYCLOPENTANECARBOXYLIC ACID DERIVATIVES AND THEIR USE AS PHARMACEUTICALS

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Page/Page column 115-116, (2010/01/29)

The present invention relates to compounds of the formula (I), wherein A, Y, Z, R3 to R6, R20 to R22 and R50 have the meanings indicated in the claims, which are valuable pharmaceutical active compounds. Specifically, they are inhibitors of the endothelial differentiation gene receptor 2 (Edg-2, EDG2), which is activated by lysophosphatidic acid (LPA) and is also termed as LPA1 receptor, and are useful for the treatment of diseases such as atherosclerosis, myocardial infarction and heart failure, for example. The invention furthermore relates to processes for the preparation of the compounds of the formula (I), their use and pharmaceutical compositions comprising them.

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