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Phosphine, 1,3-butadiene-1,4-diylidenebis[[2,4,6-tris(1,1-dimethylethyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Phosphine, 1,3-butadiene-1,4-diylidenebis[[2,4,6-tris(1,1-dimethylethyl)phenyl]-

    Cas No: 144500-96-9

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  • 144500-96-9 Structure
  • Basic information

    1. Product Name: Phosphine, 1,3-butadiene-1,4-diylidenebis[[2,4,6-tris(1,1-dimethylethyl)phenyl]-
    2. Synonyms:
    3. CAS NO:144500-96-9
    4. Molecular Formula: C40H60P2
    5. Molecular Weight: 602.864
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144500-96-9.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: Phosphine, 1,3-butadiene-1,4-diylidenebis[[2,4,6-tris(1,1-dimethylethyl)phenyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phosphine, 1,3-butadiene-1,4-diylidenebis[[2,4,6-tris(1,1-dimethylethyl)phenyl]-(144500-96-9)
    11. EPA Substance Registry System: Phosphine, 1,3-butadiene-1,4-diylidenebis[[2,4,6-tris(1,1-dimethylethyl)phenyl]-(144500-96-9)
  • 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: 144500-96-9(Hazardous Substances Data)

144500-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144500-96-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,5,0 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 144500-96:
(8*1)+(7*4)+(6*4)+(5*5)+(4*0)+(3*0)+(2*9)+(1*6)=109
109 % 10 = 9
So 144500-96-9 is a valid CAS Registry Number.

144500-96-9Relevant articles and documents

Preparation and Isomerization of 3,4-Bis(2,4,6-tri-t-butylphenylphosphinidene)cyclobutenes

Toyota, Kozo,Tashiro, Katsuya,Yoshifuji, Masaaki,Nagase, Shigeru

, p. 2297 - 2299 (1992)

(E,E)- and (E,Z)-3,4-Bis(2,4,6-tri-t-butylphenylphosphinidene)cyclobutenes were prepared by desilylation reaction of the corresponding 1,2-bis(trimethylsilyl)cyclobutenes or by thermal isomerization reaction of 1,6-bis(2,4,6-tri-t-butylphenyl)-1,6-diphosp

1λ3?2,6λ3?2-Diphospha-1,2,4,5-hexatetraen aus 1,6-Di-H-1,6-diphosphino-2,4-hexadiin

Maerkl, Gottfried,Hennig, Ruediger,Noeth, Heinrich,Schmidt, Martin

, p. 6429 - 6432 (1995)

1,6-Di-H-1,6-diphosphino-2,4-hexadiyne 5 undergoes a base-catalyzed heteropropargylic rearrangement to give 1,6-diphosphahexatetraene 3a, which forms stereoselective 3,4-diphosphamethylencyclobutene 4a by valence isomerisation.

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