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CAS

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1569272-12-3

(2-isopropyl-1,3-dithian-2-yl)(phenyl)methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1569272-12-3 Structure

  • Basic information

    1. Product Name: (2-isopropyl-1,3-dithian-2-yl)(phenyl)methanol
    2. Synonyms: (2-isopropyl-1,3-dithian-2-yl)(phenyl)methanol
    3. CAS NO:1569272-12-3
    4. Molecular Formula:
    5. Molecular Weight: 268.444
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1569272-12-3.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-isopropyl-1,3-dithian-2-yl)(phenyl)methanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2-isopropyl-1,3-dithian-2-yl)(phenyl)methanol(1569272-12-3)
    11. EPA Substance Registry System: (2-isopropyl-1,3-dithian-2-yl)(phenyl)methanol(1569272-12-3)

  • 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: 1569272-12-3(Hazardous Substances Data)

1569272-12-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1569272-12-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,9,2,7 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1569272-12:
(9*1)+(8*5)+(7*6)+(6*9)+(5*2)+(4*7)+(3*2)+(2*1)+(1*2)=193
193 % 10 = 3
So 1569272-12-3 is a valid CAS Registry Number.

1569272-12-3Relevant articles and documents

Synthesis of chiral α-diarylacetic esters by stereospecific 1,2-aryl migration promoted by in situ generated acetals from benzoins

Kothapalli, Raveendra Babu,Niddana, Ramana,Balamurugan, Rengarajan

, p. 1278 - 1281 (2014)

A simple protocol for the synthesis of α-diarylacetic esters from benzoins is described. In situ generated acetal assists rapid 1,2-aryl migration in a stereospecific manner, paving the way to make enantioenriched α-diarylacetic esters from easily accessi

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