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CAS

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1344013-07-5

{1-[3,3-bis(ethoxymethyl)cyclobutylidene]-2-methylallyl}benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1344013-07-5 Structure

  • Basic information

    1. Product Name: {1-[3,3-bis(ethoxymethyl)cyclobutylidene]-2-methylallyl}benzene
    2. Synonyms: {1-[3,3-bis(ethoxymethyl)cyclobutylidene]-2-methylallyl}benzene
    3. CAS NO:1344013-07-5
    4. Molecular Formula:
    5. Molecular Weight: 300.441
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1344013-07-5.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: {1-[3,3-bis(ethoxymethyl)cyclobutylidene]-2-methylallyl}benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: {1-[3,3-bis(ethoxymethyl)cyclobutylidene]-2-methylallyl}benzene(1344013-07-5)
    11. EPA Substance Registry System: {1-[3,3-bis(ethoxymethyl)cyclobutylidene]-2-methylallyl}benzene(1344013-07-5)

  • 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: 1344013-07-5(Hazardous Substances Data)

1344013-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1344013-07-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,4,0,1 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1344013-07:
(9*1)+(8*3)+(7*4)+(6*4)+(5*0)+(4*1)+(3*3)+(2*0)+(1*7)=105
105 % 10 = 5
So 1344013-07-5 is a valid CAS Registry Number.

1344013-07-5Downstream Products

1344013-07-5Relevant articles and documents

Synthesis of small ring-containing conjugated dienes via the coupling reaction of cyclopropyl- and cyclobutylmagnesium carbenoids with α-sulfonylallyllithiums

Kimura, Tsutomu,Inumaru, Mio,Migimatsu, Takuma,Ishigaki, Masashi,Satoh, Tsuyoshi

, p. 3961 - 3970 (2013/06/27)

A variety of allylidenecyclopropanes and allylidenecyclobutanes were synthesized via the coupling reaction of cyclopropyl- and cyclobutylmagnesium carbenoids with α-sulfonylallyllithiums. Small ring cycloalkylmagnesium carbenoids were generated from aryl

New synthesis of allylidenecyclobutanes by the reaction of cyclobutylmagnesium carbenoids with vinyl sulfones

Ishigaki, Masashi,Inumaru, Mio,Satoh, Tsuyoshi

, p. 5563 - 5566 (2011/11/07)

The reaction of cyclobutylmagnesium carbenoids, which were generated from 1-chlorocyclobutyl p-tolyl sulfoxides with EtMgCl via the sulfoxide-magnesium exchange reaction at low temperature, with carbanions derived from vinyl sulfones with n-BuLi or LDA re

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