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131470-46-7

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  • 131470-46-7 Structure

  • Basic information

    1. Product Name: 1-[tert-butoxy(phenyl)methyl]-2,3-bis(methoxycarbonyl)indolizine
    2. Synonyms: 1-[tert-butoxy(phenyl)methyl]-2,3-bis(methoxycarbonyl)indolizine
    3. CAS NO:131470-46-7
    4. Molecular Formula:
    5. Molecular Weight: 395.455
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 131470-46-7.mol
    9. Article Data: 2

  • 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: 1-[tert-butoxy(phenyl)methyl]-2,3-bis(methoxycarbonyl)indolizine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-[tert-butoxy(phenyl)methyl]-2,3-bis(methoxycarbonyl)indolizine(131470-46-7)
    11. EPA Substance Registry System: 1-[tert-butoxy(phenyl)methyl]-2,3-bis(methoxycarbonyl)indolizine(131470-46-7)

  • 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: 131470-46-7(Hazardous Substances Data)

131470-46-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131470-46-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,4,7 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 131470-46:
(8*1)+(7*3)+(6*1)+(5*4)+(4*7)+(3*0)+(2*4)+(1*6)=97
97 % 10 = 7
So 131470-46-7 is a valid CAS Registry Number.

131470-46-7Relevant articles and documents

Investigation of a green oligomer of an indolizine

Asahara, Haruyasu,Awane, Ayaka,Muragishi, Kengo,Sugimoto, Ryuichi,Saigo, Kazuhiko,Nishiwaki, Nagatoshi

, p. 259 - 273 (2018/05/14)

An indolizine-based oligomer was synthesized by stirring a solution of 1-(α-alkoxybenzyl)-indolizine derivative in chloroform at room temperature. The oligomer was characterized as an octamer; it was the main component in the obtained mixture of oligomers

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