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CAS

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1181669-50-0

2-(2-[1,3]dioxan-2-ylphenyl)cyclopropane-1,1-dicarboxylic acid dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1181669-50-0 Structure

  • Basic information

    1. Product Name: 2-(2-[1,3]dioxan-2-ylphenyl)cyclopropane-1,1-dicarboxylic acid dimethyl ester
    2. Synonyms: 2-(2-[1,3]dioxan-2-ylphenyl)cyclopropane-1,1-dicarboxylic acid dimethyl ester
    3. CAS NO:1181669-50-0
    4. Molecular Formula:
    5. Molecular Weight: 320.342
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1181669-50-0.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: 2-(2-[1,3]dioxan-2-ylphenyl)cyclopropane-1,1-dicarboxylic acid dimethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2-[1,3]dioxan-2-ylphenyl)cyclopropane-1,1-dicarboxylic acid dimethyl ester(1181669-50-0)
    11. EPA Substance Registry System: 2-(2-[1,3]dioxan-2-ylphenyl)cyclopropane-1,1-dicarboxylic acid dimethyl ester(1181669-50-0)

  • 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: 1181669-50-0(Hazardous Substances Data)

1181669-50-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1181669-50-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,1,6,6 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1181669-50:
(9*1)+(8*1)+(7*8)+(6*1)+(5*6)+(4*6)+(3*9)+(2*5)+(1*0)=170
170 % 10 = 0
So 1181669-50-0 is a valid CAS Registry Number.

1181669-50-0Relevant articles and documents

Domino synthesis of bridged bicyclic tetrahydro-1,2-oxazines: Access to stereodefined 4-aminocyclohexanols

Dias, Dwayne A.,Kerr, Michael A.

, p. 3694 - 3697 (2011/03/18)

Image Presented The intramolecular variant of the homo-[3 + 2]-dipolar cycloaddition of nitrones (generated in situ from an aldehyde and a hydroxylamine) with donor-acceptor cyclopropanes allows for the efficient synthesis of bridged tetrahydro-1,2-oxazines. This domino sequence produces adducts amenable to reductive N-O bond cleavage producing cis-1,4- aminocyclohexanols in excellent yields.

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