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CAS

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144582-67-2

Acetic acid, [(4-methylphenyl)sulfinyl]-, 1-methylethyl ester, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 144582-67-2 Structure

  • Basic information

    1. Product Name: Acetic acid, [(4-methylphenyl)sulfinyl]-, 1-methylethyl ester, (S)-
    2. Synonyms:
    3. CAS NO:144582-67-2
    4. Molecular Formula: C12H16O3S
    5. Molecular Weight: 240.323
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144582-67-2.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: Acetic acid, [(4-methylphenyl)sulfinyl]-, 1-methylethyl ester, (S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetic acid, [(4-methylphenyl)sulfinyl]-, 1-methylethyl ester, (S)-(144582-67-2)
    11. EPA Substance Registry System: Acetic acid, [(4-methylphenyl)sulfinyl]-, 1-methylethyl ester, (S)-(144582-67-2)

  • 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: 144582-67-2(Hazardous Substances Data)

144582-67-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144582-67-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,5,8 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 144582-67:
(8*1)+(7*4)+(6*4)+(5*5)+(4*8)+(3*2)+(2*6)+(1*7)=142
142 % 10 = 2
So 144582-67-2 is a valid CAS Registry Number.

144582-67-2Downstream Products

144582-67-2Relevant articles and documents

Synthesis of Optically Active α-Alkylidene-β-hydroxy-γ-methylenebutyrolactones. Isoobtusilactones and Isomahubalactones (Isomahubanolide and Isomahubenolide)

Nokami, Junzo,Ohtsuki, Hirotoshi,Sakamoto, Yasuhuko,Mitsuoka, Masayuki,Kunieda, Norio

, p. 1647 - 1650 (1992)

The title compounds were prepared via stereoselective aldol reaction of α,β-unsaturated carboxylate α-anion equivalent, derived from optically active α-(arylsulfinyl)carboxylate and bromomagnesium diisopropylamide, with propargyl aldehyde as a key step.

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