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CAS

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1158541-55-9

(R)-2-[2-(6-chloro-pyridin-2-yloxy)-1-phenyl-ethyl]-2,3-dihydro-1H-isoindole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1158541-55-9 Structure

  • Basic information

    1. Product Name: (R)-2-[2-(6-chloro-pyridin-2-yloxy)-1-phenyl-ethyl]-2,3-dihydro-1H-isoindole
    2. Synonyms: (R)-2-[2-(6-chloro-pyridin-2-yloxy)-1-phenyl-ethyl]-2,3-dihydro-1H-isoindole
    3. CAS NO:1158541-55-9
    4. Molecular Formula:
    5. Molecular Weight: 350.848
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1158541-55-9.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: (R)-2-[2-(6-chloro-pyridin-2-yloxy)-1-phenyl-ethyl]-2,3-dihydro-1H-isoindole(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-2-[2-(6-chloro-pyridin-2-yloxy)-1-phenyl-ethyl]-2,3-dihydro-1H-isoindole(1158541-55-9)
    11. EPA Substance Registry System: (R)-2-[2-(6-chloro-pyridin-2-yloxy)-1-phenyl-ethyl]-2,3-dihydro-1H-isoindole(1158541-55-9)

  • 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: 1158541-55-9(Hazardous Substances Data)

1158541-55-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1158541-55-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,8,5,4 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1158541-55:
(9*1)+(8*1)+(7*5)+(6*8)+(5*5)+(4*4)+(3*1)+(2*5)+(1*5)=159
159 % 10 = 9
So 1158541-55-9 is a valid CAS Registry Number.

1158541-55-9Downstream Products

1158541-55-9Relevant articles and documents

Spiroborate ester-mediated asymmetric synthesis of β-hydroxy ethers and its conversion to highly enantiopure β-amino ethers

Huang, Kun,Ortiz-Marciales, Margarita,Correa, Wildeliz,Pomales, Edgardo,Lopez, Xaira Y.

experimental part, p. 4195 - 4202 (2009/09/25)

(Chemical Equation Presented) Borane-mediated reduction of aryl and alkyl ketones with α-aryl- and α-pyridyloxy groups affords β-hydroxy ethers in high enantiomeric purity (up to 99% ee) and in good yield, using as catalyst 10 mol % of spiroborate ester 1

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