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CAS

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448294-94-8

(Ss,4S,5S)-4,5-diphenyl-3-(methylsulfinyl)methylisoxazoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 448294-94-8 Structure

  • Basic information

    1. Product Name: (Ss,4S,5S)-4,5-diphenyl-3-(methylsulfinyl)methylisoxazoline
    2. Synonyms:
    3. CAS NO:448294-94-8
    4. Molecular Formula:
    5. Molecular Weight: 299.393
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 448294-94-8.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: (Ss,4S,5S)-4,5-diphenyl-3-(methylsulfinyl)methylisoxazoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: (Ss,4S,5S)-4,5-diphenyl-3-(methylsulfinyl)methylisoxazoline(448294-94-8)
    11. EPA Substance Registry System: (Ss,4S,5S)-4,5-diphenyl-3-(methylsulfinyl)methylisoxazoline(448294-94-8)

  • 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: 448294-94-8(Hazardous Substances Data)

448294-94-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 448294-94-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,8,2,9 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 448294-94:
(8*4)+(7*4)+(6*8)+(5*2)+(4*9)+(3*4)+(2*9)+(1*4)=188
188 % 10 = 8
So 448294-94-8 is a valid CAS Registry Number.

448294-94-8Downstream Products

448294-94-8Relevant articles and documents

Stereoselective synthesis of 3-alkylsulfinylmethylisoxazolines and their use as chiral nucleophiles in the chain elongation of 2,3-O-isopropylidene-D-glyceraldehyde

Lopez-Sastre,Martin-Ramos,Rodriguez-Amo,Santos-Garcia,Sanz-Tejedor

, p. 4791 - 4803 (2007/10/03)

The reaction of racemic 3-methylisoxazolines and enantiomerically pure (RS)- and (SS)-methanesulfinates and (RS)- and (SS)-ethanesulfinates of 1,2:5,6-di-O-isopropylidene-D-glucofuranose allows enantiomerically pure 3-alkylsulfinylmethylisoxazolines with both absolute configurations at sulfur to be obtained. One of these has been used as a chiral nucleophile in the four carbon homologation of 2,3-O-isopropylidene-D-glyceraldehyde 17.

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