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CAS

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1458011-77-2

dimethyl 6-chloroquinoxaline-2,3-dicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1458011-77-2 Structure

  • Basic information

    1. Product Name: dimethyl 6-chloroquinoxaline-2,3-dicarboxylate
    2. Synonyms: dimethyl 6-chloroquinoxaline-2,3-dicarboxylate
    3. CAS NO:1458011-77-2
    4. Molecular Formula:
    5. Molecular Weight: 280.667
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1458011-77-2.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: dimethyl 6-chloroquinoxaline-2,3-dicarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: dimethyl 6-chloroquinoxaline-2,3-dicarboxylate(1458011-77-2)
    11. EPA Substance Registry System: dimethyl 6-chloroquinoxaline-2,3-dicarboxylate(1458011-77-2)

  • 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: 1458011-77-2(Hazardous Substances Data)

1458011-77-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1458011-77-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,8,0,1 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1458011-77:
(9*1)+(8*4)+(7*5)+(6*8)+(5*0)+(4*1)+(3*1)+(2*7)+(1*7)=152
152 % 10 = 2
So 1458011-77-2 is a valid CAS Registry Number.

1458011-77-2Downstream Products

1458011-77-2Relevant articles and documents

Hypervalent iodine(III)-promoted: N -incorporation into N -aryl vinylogous carbamates to quinoxaline diesters: Access to 1,4,5,8-tetraazaphenanthrene

Sagar,Vidaycharan, Shinde,Shinde, Anand H.,Sharada, Duddu S.

supporting information, p. 4018 - 4022 (2016/06/14)

A novel oxidative N-incorporation strategy for synthesis of quinoxaline diesters under metal-free conditions is described for the first time. The mild reaction conditions allow for this transformation via the formation of two C(sp2)-N bonds utilizing cheaply available NaN3 as the N-atom source. N-Aryl vinylogous carbamates in this study undergo azidation at enamino C(sp2)-H selectively. The robustness of this strategy is further demonstrated by the synthesis of a valuable 1,4,5,8-tetraazaphenanthrene derivative using a mild and convenient approach.

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