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((2S,3S,4R)-3,4-Bis-methoxymethoxy-tetrahydro-pyran-2-yl)-phenyl-methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 282094-26-2 Structure
  • Basic information

    1. Product Name: ((2S,3S,4R)-3,4-Bis-methoxymethoxy-tetrahydro-pyran-2-yl)-phenyl-methanone
    2. Synonyms: ((2S,3S,4R)-3,4-Bis-methoxymethoxy-tetrahydro-pyran-2-yl)-phenyl-methanone
    3. CAS NO:282094-26-2
    4. Molecular Formula:
    5. Molecular Weight: 310.347
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 282094-26-2.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: ((2S,3S,4R)-3,4-Bis-methoxymethoxy-tetrahydro-pyran-2-yl)-phenyl-methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: ((2S,3S,4R)-3,4-Bis-methoxymethoxy-tetrahydro-pyran-2-yl)-phenyl-methanone(282094-26-2)
    11. EPA Substance Registry System: ((2S,3S,4R)-3,4-Bis-methoxymethoxy-tetrahydro-pyran-2-yl)-phenyl-methanone(282094-26-2)
  • 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: 282094-26-2(Hazardous Substances Data)

282094-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 282094-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,2,0,9 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 282094-26:
(8*2)+(7*8)+(6*2)+(5*0)+(4*9)+(3*4)+(2*2)+(1*6)=142
142 % 10 = 2
So 282094-26-2 is a valid CAS Registry Number.

282094-26-2Relevant articles and documents

Design of a new bifunctional asymmetric catalyst from carbohydrates: Application to catalytic asymmetric cyanosilylation of aldehydes and acetophenone

Kanai, Motomu,Hamashima, Yoshitaka,Shibasaki, Masakatsu

, p. 2405 - 2409 (2000)

A new active Lewis acid-Lewis base bifunctional asymmetric catalyst 7 was developed using carbohydrate as a scaffold and this catalyst was applied to the asymmetric cyanosilylation of aldehydes and acetophenone. The β-Ph group at the 6-position of 7 was found to be important for a high asymmetric induction (up to 80% ee) by bringing the Al and the phosphine oxide at optimum positions for a dual activation of carbonyl compounds and TMSCN. (C) 2000 Elsevier Science Ltd.

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