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CAS

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71617-05-5

4,4,5,5,-tetramethyl-2,2,2-triphenyl-1,3,2λ(5)-dioxastibolane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 71617-05-5 Structure

  • Basic information

    1. Product Name: 4,4,5,5,-tetramethyl-2,2,2-triphenyl-1,3,2λ(5)-dioxastibolane
    2. Synonyms: 4,4,5,5,-tetramethyl-2,2,2-triphenyl-1,3,2λ(5)-dioxastibolane
    3. CAS NO:71617-05-5
    4. Molecular Formula:
    5. Molecular Weight: 469.227
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 71617-05-5.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: 4,4,5,5,-tetramethyl-2,2,2-triphenyl-1,3,2λ(5)-dioxastibolane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4,4,5,5,-tetramethyl-2,2,2-triphenyl-1,3,2λ(5)-dioxastibolane(71617-05-5)
    11. EPA Substance Registry System: 4,4,5,5,-tetramethyl-2,2,2-triphenyl-1,3,2λ(5)-dioxastibolane(71617-05-5)

  • 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: 71617-05-5(Hazardous Substances Data)

71617-05-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71617-05-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,1 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 71617-05:
(7*7)+(6*1)+(5*6)+(4*1)+(3*7)+(2*0)+(1*5)=115
115 % 10 = 5
So 71617-05-5 is a valid CAS Registry Number.

71617-05-5Downstream Products

71617-05-5Relevant articles and documents

Thermal Decomposition of Some Dioxastibolanes

Zaburdyaeva, S. N.,Fedorov, A. Yu.,Dodonov, V. A.

, p. 721 - 723 (2008/10/08)

Thermal decomposition of λ**5-dioxastibolanes Ph3SbO2R obtained from triphenylantimony and primary, secondary, and tertiary 1,2-diols is accompanied by cleavage of the endocyclic C-C bond, oxidation of the aliphatic moiety, and liberation of triphenylantimony. When the group R contains a hydrogen atom at the α-carbon atom, decomposition of the organometallic compound involves the triphenylantimony fragment, the C-C bond being retained.

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