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CAS

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1403963-72-3

(5S,6S)-4,5-dimethyl-6-phenylmorpholine-2,3-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1403963-72-3 Structure

  • Basic information

    1. Product Name: (5S,6S)-4,5-dimethyl-6-phenylmorpholine-2,3-dione
    2. Synonyms: (5S,6S)-4,5-dimethyl-6-phenylmorpholine-2,3-dione
    3. CAS NO:1403963-72-3
    4. Molecular Formula:
    5. Molecular Weight: 219.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1403963-72-3.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: (5S,6S)-4,5-dimethyl-6-phenylmorpholine-2,3-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: (5S,6S)-4,5-dimethyl-6-phenylmorpholine-2,3-dione(1403963-72-3)
    11. EPA Substance Registry System: (5S,6S)-4,5-dimethyl-6-phenylmorpholine-2,3-dione(1403963-72-3)

  • 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: 1403963-72-3(Hazardous Substances Data)

1403963-72-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1403963-72-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,3,9,6 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1403963-72:
(9*1)+(8*4)+(7*0)+(6*3)+(5*9)+(4*6)+(3*3)+(2*7)+(1*2)=153
153 % 10 = 3
So 1403963-72-3 is a valid CAS Registry Number.

1403963-72-3Downstream Products

1403963-72-3Relevant articles and documents

Reactivity of β-amino alcohols against dialkyl oxalate: Synthesis and mechanism study in the formation of substituted oxalamide and/or morpholine-2,3-dione derivatives

Testa, Maria Luisa,Zaballos, Elena,Zaragoza, Ramon J.

, p. 9583 - 9591,9 (2012)

The reactivity of various β-amino alcohols with dialkyl oxalates, in several reaction conditions, has been investigated. Linear disubstituted oxalamides were obtained with primary β-amino alcohols and linear tetrasubstituted oxalamides, or a mixture of linear tetrasubstituted oxalamides and cyclic morpholine-2,3-diones were obtained with N-substituted β-amino alcohols. A DFT study of the possible mechanism has been made. The theoretical results indicate that these reactions are not kinetically controlled, there is an equilibrium between all species and therefore follow a thermodynamic control. The different behavior between the primary β-amino alcohols and N-methyl β-amino alcohols is due to the greater stability of linear disubstituted oxalamides with respect to linear tetrasubstituted oxalamides. The energy of tetrasubstituted oxalamides is closer to the energy of the corresponding morpholine-2,3-diones.

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