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Furan, 2-decyl-5-ethyltetrahydro-, cis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 92957-59-0 Structure
  • Basic information

    1. Product Name: Furan, 2-decyl-5-ethyltetrahydro-, cis-
    2. Synonyms:
    3. CAS NO:92957-59-0
    4. Molecular Formula: C16H32O
    5. Molecular Weight:
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92957-59-0.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: Furan, 2-decyl-5-ethyltetrahydro-, cis-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Furan, 2-decyl-5-ethyltetrahydro-, cis-(92957-59-0)
    11. EPA Substance Registry System: Furan, 2-decyl-5-ethyltetrahydro-, cis-(92957-59-0)
  • 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: 92957-59-0(Hazardous Substances Data)

92957-59-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92957-59-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,5 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 92957-59:
(7*9)+(6*2)+(5*9)+(4*5)+(3*7)+(2*5)+(1*9)=180
180 % 10 = 0
So 92957-59-0 is a valid CAS Registry Number.

92957-59-0Upstream product

92957-59-0Downstream Products

92957-59-0Relevant articles and documents

IDENTIFICATION AND DETERMINATION OF 16-CARBON 2,5-DIALKYLOXOLANES IN AUTOXIDIZED n-HEXADECANE SAMPLES BY CAPILLARY GAS CHROMATOGRAPHY AND MASS SPECTROMETRY.

Zinbo,Jensen

, p. 315 - 319 (2007/10/02)

Identification and determination of isomeric 16-carbon (C//1//6) 2,5-dialkyloxolanes, formed during the autoxidation of n-hexadecane under reduced oxygen pressures, by gas chromatography/mass spectrometry (GC/MS) and capillary GC are described. A bonded phase fused silica capillary column and a 'reduced pressure' on-column injection technique have been utilized for the quantitative GC analysis. Nine chromatographic peaks have been identified and assigned to six pairs of geometric isomers of C//1//6 2,5-dialkyloxolanes based on relative retention times, stereochemistry of cis and trans isomers, and formation of characteristic five-membered ring oxonium ions formed by electron-impact fragmentation.

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