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1,1,1-Trifluoro-3-((S)-toluene-4-sulfinyl)-propan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 253608-99-0 Structure
  • Basic information

    1. Product Name: 1,1,1-Trifluoro-3-((S)-toluene-4-sulfinyl)-propan-2-one
    2. Synonyms:
    3. CAS NO:253608-99-0
    4. Molecular Formula:
    5. Molecular Weight: 250.241
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 253608-99-0.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: 1,1,1-Trifluoro-3-((S)-toluene-4-sulfinyl)-propan-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,1,1-Trifluoro-3-((S)-toluene-4-sulfinyl)-propan-2-one(253608-99-0)
    11. EPA Substance Registry System: 1,1,1-Trifluoro-3-((S)-toluene-4-sulfinyl)-propan-2-one(253608-99-0)
  • 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: 253608-99-0(Hazardous Substances Data)

253608-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 253608-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,3,6,0 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 253608-99:
(8*2)+(7*5)+(6*3)+(5*6)+(4*0)+(3*8)+(2*9)+(1*9)=150
150 % 10 = 0
So 253608-99-0 is a valid CAS Registry Number.

253608-99-0Relevant articles and documents

Synthesis of (Rc,Ss)-1,1,1-trifluoro-3-(p-molylsulfinyl)-2-propanol by an asymmetric reduction with a yeast, Yamadazyma farinosa, as a key-step

Sakai, Atsushi,Bakke, Mikio,Ohta, Hiromichi,Kosugi, Hiroshi,Sugai, Takeshi

, p. 1255 - 1256 (1999)

(Rc,Ss)-1,1,1-trifluoro-3-(p-tolysulfinyl)-2-propanol (>99% e.e.), an important reagent for the asymmetric protonation of substituted enolates, was prepared (70%) from (S)-methyl p-tolyl sulfoxide. The stereoselectivity of the Yamdazyma farinosa-catalyzed

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