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CAS

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1300740-95-7

C11H12O3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1300740-95-7 Structure

  • Basic information

    1. Product Name: C11H12O3
    2. Synonyms:
    3. CAS NO:1300740-95-7
    4. Molecular Formula:
    5. Molecular Weight: 192.214
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1300740-95-7.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: C11H12O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C11H12O3(1300740-95-7)
    11. EPA Substance Registry System: C11H12O3(1300740-95-7)

  • 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: 1300740-95-7(Hazardous Substances Data)

1300740-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1300740-95-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,0,7,4 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1300740-95:
(9*1)+(8*3)+(7*0)+(6*0)+(5*7)+(4*4)+(3*0)+(2*9)+(1*5)=107
107 % 10 = 7
So 1300740-95-7 is a valid CAS Registry Number.

1300740-95-7Downstream Products

1300740-95-7Relevant articles and documents

Palladium-catalyzed oxidative cyclization of 3-phenoxyacrylates: An approach to construct substituted benzofurans from phenols

Li, Chengliang,Zhang, Yicheng,Li, Pinhua,Wang, Lei

, p. 4692 - 4696 (2011)

In this paper, a novel and applicable synthesis of benzofurans from commercially available phenols and propiolate through the direct oxidative cyclization has been developed. In the presence of Pd(OAc)2/PPh 3 and CF3COsub

Formation of Chiral Allylic Ethers via an Enantioselective Palladium-Catalyzed Alkenylation of Acyclic Enol Ethers

Patel, Harshkumar H.,Prater, Matthew B.,Squire, Scott O.,Sigman, Matthew S.

supporting information, p. 5895 - 5898 (2018/05/14)

This report details a palladium-catalyzed process to access highly functionalized, optically active allylic aryl ethers. A number of electron-deficient alkenyl triflates underwent enantioselective and site-selective coupling with acyclic aryl enol ethers

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