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2-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-benzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 324027-23-8 Structure
  • Basic information

    1. Product Name: 2-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-benzaldehyde
    2. Synonyms: 2-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-benzaldehyde
    3. CAS NO:324027-23-8
    4. Molecular Formula:
    5. Molecular Weight: 388.582
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 324027-23-8.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: 2-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-benzaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-benzaldehyde(324027-23-8)
    11. EPA Substance Registry System: 2-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-benzaldehyde(324027-23-8)
  • 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: 324027-23-8(Hazardous Substances Data)

324027-23-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 324027-23-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,4,0,2 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 324027-23:
(8*3)+(7*2)+(6*4)+(5*0)+(4*2)+(3*7)+(2*2)+(1*3)=98
98 % 10 = 8
So 324027-23-8 is a valid CAS Registry Number.

324027-23-8Relevant articles and documents

Highly diastereoselective 5-hexenyl radical cyclizations with Lewis acids and carbohydrate scaffolds.

Enholm,Cottone,Allais

, p. 145 - 147 (2007/10/03)

[figure: see text] Carbohydrates as removable chiral scaffolds for free radical cyclizations were examined for the first time. This investigation illustrates the utility of two inexpensive carbohydrate derivatives as sources of asymmetry for 5-hexenyl rad

DIASTEREO- AND ENANTIOSELECTIVE SYNTHESIS OF 1,2-DIOLS BY VANADIUM(II) PROMOTED PINACOL CROSS COUPLING

Annunziata, Rita,Cinquini, Mauro,Cozzi, Franco,Giaroni, Paola,Benaglia, Maurizio

, p. 5737 - 5758 (2007/10/02)

The V(II) promoted pinacol cross coupling of a chiral aromatic aldehyde with achiral aliphatic aldehydes occurs to afford syn diols in up to 91:9 diastereoisomeric ratio and up to 84percent enantiomeric excess.The pinacol coupling of (S)-lactaldehyde and (R)-glyceraldehyde derivatives has also been studied and matching and mis-matching pairs have been identified.The stereochemistry of the products was established by correlation.The sense and degree of stereoselection is discussed.

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