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CAS

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1016669-27-4

C15H24O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1016669-27-4 Structure

  • Basic information

    1. Product Name: C15H24O2
    2. Synonyms: C15H24O2
    3. CAS NO:1016669-27-4
    4. Molecular Formula:
    5. Molecular Weight: 236.354
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1016669-27-4.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: C15H24O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C15H24O2(1016669-27-4)
    11. EPA Substance Registry System: C15H24O2(1016669-27-4)

  • 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: 1016669-27-4(Hazardous Substances Data)

1016669-27-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1016669-27-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,6,6,6 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1016669-27:
(9*1)+(8*0)+(7*1)+(6*6)+(5*6)+(4*6)+(3*9)+(2*2)+(1*7)=144
144 % 10 = 4
So 1016669-27-4 is a valid CAS Registry Number.

1016669-27-4Downstream Products

1016669-27-4Relevant articles and documents

In situ generation of nucleophilic allenes by the gold-catalyzed rearrangement of propargylic esters for the highly diastereoselective formation of intermolecular C(sp3)-C(sp2) bonds

Yu, Yang,Yang, Weibo,Rominger, Frank,Hashmi, A. Stephen K.

, p. 7586 - 7589 (2013)

New perspectives, in particular for the synthesis of isochromane derivatives (see scheme), are provided by the title reaction. Excellent diastereoselectivites are achieved in this reaction which proceeds through a gold-catalyzed 1,3-acyloxy migration. In some cases exclusively the Z isomer is detected. Copyright

Au-catalyzed synthesis of (1Z,3E)-2-pivaloxy-1,3-dienes from propargylic pivalates

Li, Guotao,Zhang, Guozhu,Zhang, Liming

, p. 3740 - 3741 (2008/09/21)

Propargylic pivalates with electronically unbiased internal alkynes are selectively transformed into (1Z,3E)-2-pivaloxy-1,3-dienes containing various functionalities. The unusual selectivity of 1,2-acyloxy migration over the structurally preferred 3,3-rea

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