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1350930-08-3

1-(5-methylfuran-2-yl)-1-(phenylethynyl)cycloheptane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1350930-08-3 Structure

  • Basic information

    1. Product Name: 1-(5-methylfuran-2-yl)-1-(phenylethynyl)cycloheptane
    2. Synonyms:
    3. CAS NO:1350930-08-3
    4. Molecular Formula:
    5. Molecular Weight: 264.367
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1350930-08-3.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: 1-(5-methylfuran-2-yl)-1-(phenylethynyl)cycloheptane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(5-methylfuran-2-yl)-1-(phenylethynyl)cycloheptane(1350930-08-3)
    11. EPA Substance Registry System: 1-(5-methylfuran-2-yl)-1-(phenylethynyl)cycloheptane(1350930-08-3)

  • 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: 1350930-08-3(Hazardous Substances Data)

1350930-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1350930-08-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,0,9,3 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1350930-08:
(9*1)+(8*3)+(7*5)+(6*0)+(5*9)+(4*3)+(3*0)+(2*0)+(1*8)=133
133 % 10 = 3
So 1350930-08-3 is a valid CAS Registry Number.

1350930-08-3Downstream Products

1350930-08-3Relevant articles and documents

Waste-free catalytic propargylation/allenylation of aryl and heteroaryl nucleophiles and synthesis of naphthopyrans

McCubbin, J. Adam,Nassar, Costa,Krokhin, Oleg V.

, p. 3152 - 3160 (2011)

A general method for the substitution of propargylic alcohols with electron-rich aromatic carbocycles and heterocycles has been developed. The reaction occurs under simple, mild conditions, and employs an inexpensive environmentally benign and recoverable

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