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(4R,αS)-4-(hexadecyloxymethyl)-3-(α-methylbenzyl)oxazolidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1353577-09-9 Structure
  • Basic information

    1. Product Name: (4R,αS)-4-(hexadecyloxymethyl)-3-(α-methylbenzyl)oxazolidin-2-one
    2. Synonyms: (4R,αS)-4-(hexadecyloxymethyl)-3-(α-methylbenzyl)oxazolidin-2-one
    3. CAS NO:1353577-09-9
    4. Molecular Formula:
    5. Molecular Weight: 445.686
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1353577-09-9.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: (4R,αS)-4-(hexadecyloxymethyl)-3-(α-methylbenzyl)oxazolidin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4R,αS)-4-(hexadecyloxymethyl)-3-(α-methylbenzyl)oxazolidin-2-one(1353577-09-9)
    11. EPA Substance Registry System: (4R,αS)-4-(hexadecyloxymethyl)-3-(α-methylbenzyl)oxazolidin-2-one(1353577-09-9)
  • 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: 1353577-09-9(Hazardous Substances Data)

1353577-09-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1353577-09-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,3,5,7 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1353577-09:
(9*1)+(8*3)+(7*5)+(6*3)+(5*5)+(4*7)+(3*7)+(2*0)+(1*9)=169
169 % 10 = 9
So 1353577-09-9 is a valid CAS Registry Number.

1353577-09-9Relevant articles and documents

Total synthesis of (R)-(-)-actisonitrile via O-alkylation of optically active 4-hydroxymethyloxazolidin-2-one derivative

Sugiyama, Shigeo,Ishida, Akihiro,Tsuchida, Moeko,Ishii, Keitaro

experimental part, p. 1918 - 1923 (2012/02/05)

The enantioselective synthesis of (R)-(-)-actisonitrile 1 has been achieved via O-alkylation of (4R,αS)-4-hydroxymethyl-3-(α-methylbenzyl) oxazolidin-2-one (αS)-4 with 1-iodohexadecane in the presence of CsOH in DMF. Under these reaction conditions, the O

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