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123133-04-0

4-carboxyphenyl 2,4,6-tri-t-butylphenyl selenide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 123133-04-0 Structure

  • Basic information

    1. Product Name: 4-carboxyphenyl 2,4,6-tri-t-butylphenyl selenide
    2. Synonyms:
    3. CAS NO:123133-04-0
    4. Molecular Formula:
    5. Molecular Weight: 445.504
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 123133-04-0.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-carboxyphenyl 2,4,6-tri-t-butylphenyl selenide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-carboxyphenyl 2,4,6-tri-t-butylphenyl selenide(123133-04-0)
    11. EPA Substance Registry System: 4-carboxyphenyl 2,4,6-tri-t-butylphenyl selenide(123133-04-0)

  • 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: 123133-04-0(Hazardous Substances Data)

123133-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123133-04-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,1,3 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 123133-04:
(8*1)+(7*2)+(6*3)+(5*1)+(4*3)+(3*3)+(2*0)+(1*4)=70
70 % 10 = 0
So 123133-04-0 is a valid CAS Registry Number.

123133-04-0Relevant articles and documents

Synthesis and Absolute Configuration of Optically Active Selenoxides. X-Ray Molecular Structure of (-)Se-4-Menthyloxycarbonylphenyl 2,4,6-Tri-isopropylphenyl Selenoxide

Shimizu, Toshio,Kikuchi, Koichi,Ishikawa, Yoshimitsu,Ikemoto, Isao,Kobayashi, Michio,Kamigata, Nobumasa

, p. 597 - 602 (2007/10/02)

Enantiomerically pure, stable 4-(methoxycarbonyl)phenyl 2,4,6-tri-isopropylphenyl selenoxide (-)-3 was isolated by fractional recrystallization of diastereomeric 4-phenyl 2,4,6-tri-isopropylphenyl selenoxide dia.-(1) followed by removal of the chiral source.The absolute configuration around the selenium atom was determined by X-ray crystallographic analysis of diastereomerically pure selenoxide (-)Se-(1).

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