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CAS

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1402159-64-1

dimethyl 5,6,7,8-tetrachloro-1,4-dihydronaphthalene-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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  • 1402159-64-1 Structure

  • Basic information

    1. Product Name: dimethyl 5,6,7,8-tetrachloro-1,4-dihydronaphthalene-2,3-dicarboxylate
    2. Synonyms: dimethyl 5,6,7,8-tetrachloro-1,4-dihydronaphthalene-2,3-dicarboxylate
    3. CAS NO:1402159-64-1
    4. Molecular Formula:
    5. Molecular Weight: 384.043
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1402159-64-1.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 5,6,7,8-tetrachloro-1,4-dihydronaphthalene-2,3-dicarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: dimethyl 5,6,7,8-tetrachloro-1,4-dihydronaphthalene-2,3-dicarboxylate(1402159-64-1)
    11. EPA Substance Registry System: dimethyl 5,6,7,8-tetrachloro-1,4-dihydronaphthalene-2,3-dicarboxylate(1402159-64-1)

  • 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: 1402159-64-1(Hazardous Substances Data)

1402159-64-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1402159-64-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,2,1,5 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1402159-64:
(9*1)+(8*4)+(7*0)+(6*2)+(5*1)+(4*5)+(3*9)+(2*6)+(1*4)=121
121 % 10 = 1
So 1402159-64-1 is a valid CAS Registry Number.

1402159-64-1Downstream Products

1402159-64-1Relevant articles and documents

Diversity oriented approach to polycyclic compounds through the diels-alder reaction and the Suzuki coupling

Kotha, Sambasivarao,Misra, Shilpi,Srinivas, Venu

, p. 4052 - 4062 (2012/09/07)

A diversity oriented strategy has been demonstrated to deliver small "drug like" molecules using alkylation, Diels-Alder reaction, and Suzuki-Miyaura cross-coupling as key steps. This methodology allows access a wide range of molecules using simple scaffolds such as indanes, tetralins and tetrahydroisoquinolines, which can enhance the chemical space for potential therapeutic molecules.

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