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CAS

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87184-65-4

trans-2-(p-tolylthio)cyclopentanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 87184-65-4 Structure

  • Basic information

    1. Product Name: trans-2-(p-tolylthio)cyclopentanol
    2. Synonyms: trans-2-(p-tolylthio)cyclopentanol
    3. CAS NO:87184-65-4
    4. Molecular Formula:
    5. Molecular Weight: 208.324
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 87184-65-4.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: trans-2-(p-tolylthio)cyclopentanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: trans-2-(p-tolylthio)cyclopentanol(87184-65-4)
    11. EPA Substance Registry System: trans-2-(p-tolylthio)cyclopentanol(87184-65-4)

  • 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: 87184-65-4(Hazardous Substances Data)

87184-65-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87184-65-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,1,8 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 87184-65:
(7*8)+(6*7)+(5*1)+(4*8)+(3*4)+(2*6)+(1*5)=164
164 % 10 = 4
So 87184-65-4 is a valid CAS Registry Number.

87184-65-4Relevant articles and documents

An efficient catalyst for ring opening of epoxides with phenol and thiophenol under solvent-free conditions

Lu, Hong-Fei,Zhou, Jun-Tao,Cheng, He-Long,Sun, Lei-Lei,Yang, Fei-Fei,Wu, Run-Ze,Gao, Yu-Hua,Luo, Zhi-Bin

, p. 11174 - 11184 (2014/01/06)

An efficient and rapid procedure for ring opening reaction of various epoxides with phenol and thiophenol derivatives was developed. The procedure can be obtained at room temperature under solvent-free condition in presence of (C4H12N2)2[BiCl6] Cl·H2O (1 mol %). This catalyst can be reused several times without significant loss of activity.

Convenient preparation of ytterbium(III) chalcogenolate complexes by insertion of ytterbium into chalcogen-chalcogen bonds. Application in the ring-opening of epoxides

Dowsland, Jennifer,McKerlie, Fiona,Procter, David J.

, p. 4923 - 4927 (2007/10/03)

Convenient conditions are reported for the preparation of ytterbium(III) chalcogenolate complexes by insertion of ytterbium metal into the chalcogen- chalcogen bond of disulfides, diselenides, and ditellurides. The resulting complexes have been found to t

Preparation and Stereochemistry of Methylation of Some Cycloalkyl Sulfones

Rothberg, Irvin,Sundoro, Boby,Balanikas, George,Kirsch, Sheldon

, p. 4345 - 4348 (2007/10/02)

3-((4-methylphenyl)sulfonyl)cyclohexanols (2, 3), 3-((4-methylphenyl)sulfonyl)cyclopentanols (7, 8), and 2-((4-methylphenyl)sulfonyl)cyclopentanols (12, 15) and their tetrahydropyranyl ether derivatives were prepared.Attempted methylation of the tetrahydr

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