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141036-65-9

Benzenepropanol, a-[[(4-methylphenyl)thio]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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  • 141036-65-9 Structure

  • Basic information

    1. Product Name: Benzenepropanol, a-[[(4-methylphenyl)thio]methyl]-, (R)-
    2. Synonyms:
    3. CAS NO:141036-65-9
    4. Molecular Formula: C17H20OS
    5. Molecular Weight: 272.411
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 141036-65-9.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: Benzenepropanol, a-[[(4-methylphenyl)thio]methyl]-, (R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenepropanol, a-[[(4-methylphenyl)thio]methyl]-, (R)-(141036-65-9)
    11. EPA Substance Registry System: Benzenepropanol, a-[[(4-methylphenyl)thio]methyl]-, (R)-(141036-65-9)

  • 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: 141036-65-9(Hazardous Substances Data)

141036-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141036-65-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,0,3 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 141036-65:
(8*1)+(7*4)+(6*1)+(5*0)+(4*3)+(3*6)+(2*6)+(1*5)=89
89 % 10 = 9
So 141036-65-9 is a valid CAS Registry Number.

141036-65-9Relevant articles and documents

Asymmetric Synthesis of (-) (R) Yashabushiketol

Solladie, Guy,Ziani-Cherif, Chewki,Jesser, Francis

, p. 931 - 934 (2007/10/02)

(-)(R) Yashabushiketol was prepared from the epoxide 4 readily available in both configurations by reduction of β-ketosulfoxides.

REDUCTION OF β-HYDROXYSULFOXIDES: APPLICATION TO THE SYNTHESIS OF OPTICALLY ACTIVE EPOXIDES

Solladie, Guy,Demailly, Gilles,Greck, Christine

, p. 435 - 438 (2007/10/02)

β-hydroxysulfoxides of opposite stereochemistry can be prepared in very high diastereoisomeric excesses (90 to 95 percent) by reduction of β-ketosulfoxides with DIBAL or DIBAL/ZnCl2.A very efficient method to transform these reduction products into optically active epoxides is also described.

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