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(R)-5-ethyl-1,3-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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  • 947683-08-1 Structure
  • Basic information

    1. Product Name: (R)-5-ethyl-1,3-oxazolidin-2-one
    2. Synonyms: (R)-5-ethyl-1,3-oxazolidin-2-one
    3. CAS NO:947683-08-1
    4. Molecular Formula:
    5. Molecular Weight: 115.132
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 947683-08-1.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)-5-ethyl-1,3-oxazolidin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-5-ethyl-1,3-oxazolidin-2-one(947683-08-1)
    11. EPA Substance Registry System: (R)-5-ethyl-1,3-oxazolidin-2-one(947683-08-1)
  • 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: 947683-08-1(Hazardous Substances Data)

947683-08-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 947683-08-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,7,6,8 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 947683-08:
(8*9)+(7*4)+(6*7)+(5*6)+(4*8)+(3*3)+(2*0)+(1*8)=221
221 % 10 = 1
So 947683-08-1 is a valid CAS Registry Number.

947683-08-1Downstream Products

947683-08-1Relevant articles and documents

Formation of enantiopure 5-substituted oxazolidinones through enzyme-catalysed kinetic resolution of epoxides

Elenkov, Maja Majeric,Tang, Lixia,Meetsma, Auke,Hauer, Bernhard,Janssen, Dick B.

, p. 2417 - 2420 (2008)

(Chemical Equation Presented) Halohydrin dehalogenase from Agrobacterium radiobacter catalyzed the enantioselective ring opening of terminal epoxides with cyanate as a nucleophile, yielding 5-substituted oxazolidinones in high yields and with high enantiopurity (69-98% ee). This is the first example of the biocatalytic conversion of a range of epoxides to the corresponding oxazolidinones.

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