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CAS

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128949-52-0

Pyridine, 2-[[(4-methylphenyl)sulfinyl]methyl]-, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 128949-52-0 Structure

  • Basic information

    1. Product Name: Pyridine, 2-[[(4-methylphenyl)sulfinyl]methyl]-, (R)-
    2. Synonyms:
    3. CAS NO:128949-52-0
    4. Molecular Formula: C13H13NOS
    5. Molecular Weight: 231.318
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 128949-52-0.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: Pyridine, 2-[[(4-methylphenyl)sulfinyl]methyl]-, (R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Pyridine, 2-[[(4-methylphenyl)sulfinyl]methyl]-, (R)-(128949-52-0)
    11. EPA Substance Registry System: Pyridine, 2-[[(4-methylphenyl)sulfinyl]methyl]-, (R)-(128949-52-0)

  • 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: 128949-52-0(Hazardous Substances Data)

128949-52-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128949-52-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,9,4 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 128949-52:
(8*1)+(7*2)+(6*8)+(5*9)+(4*4)+(3*9)+(2*5)+(1*2)=170
170 % 10 = 0
So 128949-52-0 is a valid CAS Registry Number.

128949-52-0Relevant articles and documents

Enzymatic kinetic resolution of chiral sulfoxides-an enantiocomplementary approach

Nosek, Vladimír,Mí?ek, Ji?í

supporting information, p. 10480 - 10483 (2019/09/07)

A new enzymatic assay for the preparation of chiral sulfoxides that is enantiocomplementary to the known (S)-enantiomer-reducing activity of methionine sulfoxide reductase A (MsrA) is described. To this end, we have utilized the enzyme DMSO reductase (DmsABC), recently discovered by us being highly upregulated in stationary phase E. coli bacteria.

Synthesis of new optically active sulfoxides with chelating properties

Baldenius, Kai-U.,Kagan, Henri B.

, p. 597 - 610 (2007/10/02)

Access to enantiomerically pure 2-pyridinylmethyl sulfoxides and β-imino sulfoxides was sought.The latter were obtained in tautomeric mixtures with their enamines by condensation of optically active β-keto sulfoxides with primary amines. 2-Pyridinylmethyl

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