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2,2,4,4-tetramethyl-1-phenylpentane-1,5-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 247090-26-2 Structure
  • Basic information

    1. Product Name: 2,2,4,4-tetramethyl-1-phenylpentane-1,5-diol
    2. Synonyms: 2,2,4,4-tetramethyl-1-phenylpentane-1,5-diol
    3. CAS NO:247090-26-2
    4. Molecular Formula:
    5. Molecular Weight: 236.354
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 247090-26-2.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: 2,2,4,4-tetramethyl-1-phenylpentane-1,5-diol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2,4,4-tetramethyl-1-phenylpentane-1,5-diol(247090-26-2)
    11. EPA Substance Registry System: 2,2,4,4-tetramethyl-1-phenylpentane-1,5-diol(247090-26-2)
  • 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: 247090-26-2(Hazardous Substances Data)

247090-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 247090-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,7,0,9 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 247090-26:
(8*2)+(7*4)+(6*7)+(5*0)+(4*9)+(3*0)+(2*2)+(1*6)=132
132 % 10 = 2
So 247090-26-2 is a valid CAS Registry Number.

247090-26-2Relevant articles and documents

Rearrangement of the carbanion generated from a tied-back 1,2,4- trithiolane oxide (6,7,8-trithiabicyclo[3.2.1]octane 6-oxide)

Ishii, Akihiko,Nakaniwa, Tetsuya,Umezawa, Kazuyo,Nakayama, Juzo

, p. 10341 - 10350 (2007/10/03)

Treatment of 2,2,4,4-tetramethyl-6,7,8-trithiabicyclo[3.2.1]octane 6- exo-oxide (3) with LDA, followed by treatment with D2O, R1 (R = Me, Et), and 2-PrBr, yielded the deuterated starting compound (3-d), bicyclic 1,3- dithietane oxides (12, 13),

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