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CAS

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241818-05-3

tert-Butyl-dimethyl-((S)-1-phenyl-butoxy)-silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 241818-05-3 Structure

  • Basic information

    1. Product Name: tert-Butyl-dimethyl-((S)-1-phenyl-butoxy)-silane
    2. Synonyms: tert-Butyl-dimethyl-((S)-1-phenyl-butoxy)-silane
    3. CAS NO:241818-05-3
    4. Molecular Formula:
    5. Molecular Weight: 264.483
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 241818-05-3.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: tert-Butyl-dimethyl-((S)-1-phenyl-butoxy)-silane(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-Butyl-dimethyl-((S)-1-phenyl-butoxy)-silane(241818-05-3)
    11. EPA Substance Registry System: tert-Butyl-dimethyl-((S)-1-phenyl-butoxy)-silane(241818-05-3)

  • 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: 241818-05-3(Hazardous Substances Data)

241818-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 241818-05-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,1,8,1 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 241818-05:
(8*2)+(7*4)+(6*1)+(5*8)+(4*1)+(3*8)+(2*0)+(1*5)=123
123 % 10 = 3
So 241818-05-3 is a valid CAS Registry Number.

241818-05-3Downstream Products

241818-05-3Relevant articles and documents

A New Approach to Remote Asymmetric Induction in the Diastereoselective Reduction of γ-Keto Esters by Use of a Chiral Podand as Chiral Auxiliary

Tamai, Yasufumi,Koike, Shinji,Ogura, Atsuhiko,Miyano, Sotaro

, p. 799 - 800 (2007/10/02)

An efficient 1,7-asymmetric induction was achieved with up to 82percent diastereoisomeric excess (d.e.) in the diastereoselective reduction of the γ-keto ester 4 and o-acetylbenzoate 6 using a chiral podand 2 as a chiral auxiliary.

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