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1426332-84-4

(3S,5S)-3-(4-benzyl-5-morpholinooxazol-2-yl)-3-methyl-5-phenylmorpholin-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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  • 1426332-84-4 Structure

  • Basic information

    1. Product Name: (3S,5S)-3-(4-benzyl-5-morpholinooxazol-2-yl)-3-methyl-5-phenylmorpholin-2-one
    2. Synonyms: (3S,5S)-3-(4-benzyl-5-morpholinooxazol-2-yl)-3-methyl-5-phenylmorpholin-2-one
    3. CAS NO:1426332-84-4
    4. Molecular Formula:
    5. Molecular Weight: 433.507
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1426332-84-4.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: (3S,5S)-3-(4-benzyl-5-morpholinooxazol-2-yl)-3-methyl-5-phenylmorpholin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3S,5S)-3-(4-benzyl-5-morpholinooxazol-2-yl)-3-methyl-5-phenylmorpholin-2-one(1426332-84-4)
    11. EPA Substance Registry System: (3S,5S)-3-(4-benzyl-5-morpholinooxazol-2-yl)-3-methyl-5-phenylmorpholin-2-one(1426332-84-4)

  • 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: 1426332-84-4(Hazardous Substances Data)

1426332-84-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1426332-84-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,6,3,3 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1426332-84:
(9*1)+(8*4)+(7*2)+(6*6)+(5*3)+(4*3)+(3*2)+(2*8)+(1*4)=144
144 % 10 = 4
So 1426332-84-4 is a valid CAS Registry Number.

1426332-84-4Downstream Products

1426332-84-4Relevant articles and documents

Catalytic ugi-type condensation of α-isocyanoacetamide and chiral cyclic imine: Access to asymmetric construction of several heterocycles

Xia, Liang,Li, Sheng,Chen, Ruijiao,Liu, Kai,Chen, Xiaochuan

, p. 3120 - 3131 (2013)

Several novel heterocycles have been constructed asymmetrically on the basis of a catalytic Ugi-type condensation of α-isocyanoacetamide and chiral cyclic imine. The combination of phenylphosphilic acid and trifluoroethanol is exploited to promote an Ugi-type reaction with α-isocyanoacetamide for the first time. By means of this reaction, chiral 3-oxazolyl morpholin-2-one/piperazin-2-one derivatives are synthesized with high yields and excellent stereoselectivities. As electron-rich azadienes, these condensation products are further transformed to fused tricyclic frameworks by treatment with appropriate dienophiles such as maleic anhydride and unsaturated acyl chlorides via domino processes. Moreover, a one-pot, three-component synthesis of the chiral tricyclic frameworks from isocyanoacetamide, imine, and maleic anhydride is also feasible.

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