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88911-00-6

(4S,5S)-4-(2-Imidazol-1-yl-2-oxo-ethyl)-5-trityloxymethyl-cyclopent-2-enone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 88911-00-6 Structure

  • Basic information

    1. Product Name: (4S,5S)-4-(2-Imidazol-1-yl-2-oxo-ethyl)-5-trityloxymethyl-cyclopent-2-enone
    2. Synonyms:
    3. CAS NO:88911-00-6
    4. Molecular Formula:
    5. Molecular Weight: 462.548
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 88911-00-6.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: (4S,5S)-4-(2-Imidazol-1-yl-2-oxo-ethyl)-5-trityloxymethyl-cyclopent-2-enone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4S,5S)-4-(2-Imidazol-1-yl-2-oxo-ethyl)-5-trityloxymethyl-cyclopent-2-enone(88911-00-6)
    11. EPA Substance Registry System: (4S,5S)-4-(2-Imidazol-1-yl-2-oxo-ethyl)-5-trityloxymethyl-cyclopent-2-enone(88911-00-6)

  • 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: 88911-00-6(Hazardous Substances Data)

88911-00-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88911-00-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,1 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88911-00:
(7*8)+(6*8)+(5*9)+(4*1)+(3*1)+(2*0)+(1*0)=156
156 % 10 = 6
So 88911-00-6 is a valid CAS Registry Number.

88911-00-6Relevant articles and documents

PERHYDROPENTALENONE EQUIVALENT FROM COREY'S LACTONE

Mongelli, N.,Andreoni, A.,Zuliani, L.,Gandolfi, C.A.

, p. 3527 - 3530 (2007/10/02)

2-Oxa-bicyclooctane-3,7-diones work as a δ-oxo-β,γ-cyclopentenyl-acetic acid substrates when submitted to the Barco procedure in the synthesis of perhydropentalenones.

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