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1449385-79-8

C11H16O3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1449385-79-8 Structure

  • Basic information

    1. Product Name: C11H16O3
    2. Synonyms: C11H16O3
    3. CAS NO:1449385-79-8
    4. Molecular Formula:
    5. Molecular Weight: 196.246
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1449385-79-8.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: C11H16O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C11H16O3(1449385-79-8)
    11. EPA Substance Registry System: C11H16O3(1449385-79-8)

  • 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: 1449385-79-8(Hazardous Substances Data)

1449385-79-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1449385-79-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,9,3,8 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1449385-79:
(9*1)+(8*4)+(7*4)+(6*9)+(5*3)+(4*8)+(3*5)+(2*7)+(1*9)=208
208 % 10 = 8
So 1449385-79-8 is a valid CAS Registry Number.

1449385-79-8Downstream Products

1449385-79-8Relevant articles and documents

Cyclopentannulation of Conjugated Enones Using a Vinyldiazomethane-Based Reagent

Del Bel, Matthew,Rovira, Alexander,Guerrero, Carlos A.

, p. 12188 - 12191 (2013)

Herein, we describe a two-step method for the cyclopentannulation of conjugated enones using methyl 3-(tert-butyldimethylsilyloxy)-2-diazo-3- butenoate (1) as a bifunctional reagent. The enol silane and stabilized diazoalkane functionalities are exploited independently in sequential Mukaiyama-Michael and diastereoselective α,α′-diketone coupling. Di-, tri-, and tetrasubstituted enones are amenable to annulation under this protocol. Overall, this chemistry is an effective surrogate for a substituted acetone 1,3-dipole .

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