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2-Cyclopent-2-eneylbenzyl alcohol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 126087-58-9 Structure
  • Basic information

    1. Product Name: 2-Cyclopent-2-eneylbenzyl alcohol
    2. Synonyms: 2-Cyclopent-2-eneylbenzyl alcohol
    3. CAS NO:126087-58-9
    4. Molecular Formula:
    5. Molecular Weight: 174.243
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 126087-58-9.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: 2-Cyclopent-2-eneylbenzyl alcohol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Cyclopent-2-eneylbenzyl alcohol(126087-58-9)
    11. EPA Substance Registry System: 2-Cyclopent-2-eneylbenzyl alcohol(126087-58-9)
  • 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: 126087-58-9(Hazardous Substances Data)

126087-58-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126087-58-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,0,8 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 126087-58:
(8*1)+(7*2)+(6*6)+(5*0)+(4*8)+(3*7)+(2*5)+(1*8)=129
129 % 10 = 9
So 126087-58-9 is a valid CAS Registry Number.

126087-58-9Downstream Products

126087-58-9Relevant articles and documents

IMPROVED PROCEDURES FOR THE PALLADIUM-CATALYZED INTERMOLECULAR ARYLATION OF CYCLIC ALKENES

Larock, Richard C.,Gong, William H.,Baker, Bruce E.

, p. 2603 - 2606 (2007/10/02)

Improved procedures for the palladium-catalyzed, intermolecular, allylic crosscoupling of aryl halides and cyclic alkenes inhibit double-bond isomerization and accommodate many important functional groups.

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