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3-<(E)-3-(benzyloxy)-1-octenyl>cyclopentanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76042-92-7 Structure
  • Basic information

    1. Product Name: 3-<(E)-3-(benzyloxy)-1-octenyl>cyclopentanone
    2. Synonyms: 3-<(E)-3-(benzyloxy)-1-octenyl>cyclopentanone
    3. CAS NO:76042-92-7
    4. Molecular Formula:
    5. Molecular Weight: 300.441
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76042-92-7.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: 3-<(E)-3-(benzyloxy)-1-octenyl>cyclopentanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-<(E)-3-(benzyloxy)-1-octenyl>cyclopentanone(76042-92-7)
    11. EPA Substance Registry System: 3-<(E)-3-(benzyloxy)-1-octenyl>cyclopentanone(76042-92-7)
  • 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: 76042-92-7(Hazardous Substances Data)

76042-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76042-92-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,4 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 76042-92:
(7*7)+(6*6)+(5*0)+(4*4)+(3*2)+(2*9)+(1*2)=127
127 % 10 = 7
So 76042-92-7 is a valid CAS Registry Number.

76042-92-7Downstream Products

76042-92-7Relevant articles and documents

A practical, general three-component coupling approach to prostaglandin and non-prostaglandin-related skeleta

Lipshutz, Bruce H.,Wood, Michael R.

, p. 11689 - 11702 (1994)

Starting with a terminal alkyne, a one-pot, six-step sequence has been developed which results in prostaglandin and related skeleta in high yields. The method involves a transmetalation between organozirconium and cuprate species, as well as another betwe

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