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1296719-10-2

tert-butyl[1-(2,5-dimethoxyphenyl)-2-nitropropoxy]dimethylsilane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • tert-butyl[1-(2,5-dimethoxyphenyl)-2-nitropropoxy]dimethylsilane

    Cas No: 1296719-10-2

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  • 1296719-10-2 Structure

  • Basic information

    1. Product Name: tert-butyl[1-(2,5-dimethoxyphenyl)-2-nitropropoxy]dimethylsilane
    2. Synonyms: tert-butyl[1-(2,5-dimethoxyphenyl)-2-nitropropoxy]dimethylsilane
    3. CAS NO:1296719-10-2
    4. Molecular Formula:
    5. Molecular Weight: 355.506
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1296719-10-2.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: tert-butyl[1-(2,5-dimethoxyphenyl)-2-nitropropoxy]dimethylsilane(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl[1-(2,5-dimethoxyphenyl)-2-nitropropoxy]dimethylsilane(1296719-10-2)
    11. EPA Substance Registry System: tert-butyl[1-(2,5-dimethoxyphenyl)-2-nitropropoxy]dimethylsilane(1296719-10-2)

  • 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: 1296719-10-2(Hazardous Substances Data)

1296719-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1296719-10-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,6,7,1 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1296719-10:
(9*1)+(8*2)+(7*9)+(6*6)+(5*7)+(4*1)+(3*9)+(2*1)+(1*0)=192
192 % 10 = 2
So 1296719-10-2 is a valid CAS Registry Number.

1296719-10-2Relevant articles and documents

Efficient access to C1- and C3-functionalized isoquinolines: Towards potential lanthanide ligands

Caille, Fabien,Buron, Frederic,Toth, Eva,Suzenet, Franck

experimental part, p. 2120 - 2127 (2011/05/09)

Highly substituted isoquinolines have been synthesized by two different pathways using either a Pictet-Grams or a Bischler-Napieralski approach. While the first synthesis afforded C1-functionalizable 1,3-dimethylisoquinoline derivatives, the second approa

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