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CAS

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124549-82-2

2α-(3-Indolyl)-4,6,6-trimethylcyclohex-3-ene-1β-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124549-82-2 Structure

  • Basic information

    1. Product Name: 2α-(3-Indolyl)-4,6,6-trimethylcyclohex-3-ene-1β-carboxylic acid
    2. Synonyms:
    3. CAS NO:124549-82-2
    4. Molecular Formula:
    5. Molecular Weight: 283.37
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124549-82-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2α-(3-Indolyl)-4,6,6-trimethylcyclohex-3-ene-1β-carboxylic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2α-(3-Indolyl)-4,6,6-trimethylcyclohex-3-ene-1β-carboxylic acid(124549-82-2)
    11. EPA Substance Registry System: 2α-(3-Indolyl)-4,6,6-trimethylcyclohex-3-ene-1β-carboxylic acid(124549-82-2)

  • 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: 124549-82-2(Hazardous Substances Data)

124549-82-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124549-82-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,5,4 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 124549-82:
(8*1)+(7*2)+(6*4)+(5*5)+(4*4)+(3*9)+(2*8)+(1*2)=132
132 % 10 = 2
So 124549-82-2 is a valid CAS Registry Number.

124549-82-2Relevant articles and documents

A general approach to the total synthesis of yuehchukene and its analogues. A novel anti-implantation agent

Kutney, James Peter,Lopez, Francisco Javier,Huang, Shyl-Pyng,Kurobe, Hiroshi

, p. 565 - 572 (2007/10/02)

A versatile synthetic strategy has been developed for the synthesis of the interesting dimeric indole natural product yuehchukene (17) and its epimer, 6a-epi-yuehchukene (22). Due to the anti-implantation activity associated with 17, it is important to develop a synthetic route not only to 17, but to a family of yuehchukene analogues with better chemical stability and/or elevated biological activity. The strategy described here and which utilizes the readily available and inexpensive isophorone (1) satisfies these requirements.

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