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CAS

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201543-16-0

(R)-3-Biphenyl-4-ylmethyl-5,5-dimethyl-isoxazolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 201543-16-0 Structure

  • Basic information

    1. Product Name: (R)-3-Biphenyl-4-ylmethyl-5,5-dimethyl-isoxazolidine
    2. Synonyms: (R)-3-Biphenyl-4-ylmethyl-5,5-dimethyl-isoxazolidine
    3. CAS NO:201543-16-0
    4. Molecular Formula:
    5. Molecular Weight: 267.371
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 201543-16-0.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)-3-Biphenyl-4-ylmethyl-5,5-dimethyl-isoxazolidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-3-Biphenyl-4-ylmethyl-5,5-dimethyl-isoxazolidine(201543-16-0)
    11. EPA Substance Registry System: (R)-3-Biphenyl-4-ylmethyl-5,5-dimethyl-isoxazolidine(201543-16-0)

  • 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: 201543-16-0(Hazardous Substances Data)

201543-16-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 201543-16-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,5,4 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 201543-16:
(8*2)+(7*0)+(6*1)+(5*5)+(4*4)+(3*3)+(2*1)+(1*6)=80
80 % 10 = 0
So 201543-16-0 is a valid CAS Registry Number.

201543-16-0Downstream Products

201543-16-0Relevant articles and documents

Synthesis of chiral 3-substituted isoxazolidines

Farr, Roger N.

, p. 195 - 196 (2007/10/03)

The synthesis of chiral (>98% ee) 3-substituted isoxazolidines has been achieved. Glycidyl tosylate was utilized to establish the desired stereochemistry in a 'double grignard' reaction sequence. Mesylate displacement followed by acid-catalyzed cyclization allows the parent isoxazolidines to be obtained.

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