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1380095-36-2

(4R,5S)-5-(4-methoxybenzoyl)-4-(4-methoxyphenyl)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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  • 1380095-36-2 Structure

  • Basic information

    1. Product Name: (4R,5S)-5-(4-methoxybenzoyl)-4-(4-methoxyphenyl)oxazolidin-2-one
    2. Synonyms: (4R,5S)-5-(4-methoxybenzoyl)-4-(4-methoxyphenyl)oxazolidin-2-one
    3. CAS NO:1380095-36-2
    4. Molecular Formula:
    5. Molecular Weight: 327.337
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1380095-36-2.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,5S)-5-(4-methoxybenzoyl)-4-(4-methoxyphenyl)oxazolidin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4R,5S)-5-(4-methoxybenzoyl)-4-(4-methoxyphenyl)oxazolidin-2-one(1380095-36-2)
    11. EPA Substance Registry System: (4R,5S)-5-(4-methoxybenzoyl)-4-(4-methoxyphenyl)oxazolidin-2-one(1380095-36-2)

  • 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: 1380095-36-2(Hazardous Substances Data)

1380095-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1380095-36-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,0,9 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1380095-36:
(9*1)+(8*3)+(7*8)+(6*0)+(5*0)+(4*9)+(3*5)+(2*3)+(1*6)=152
152 % 10 = 2
So 1380095-36-2 is a valid CAS Registry Number.

1380095-36-2Relevant articles and documents

Hydrogen-bond-mediated asymmetric cascade reaction of stable sulfur ylides with nitroolefins: Scope, application and mechanism

Lu, Liang-Qiu,Li, Fang,An, Jing,Cheng, Ying,Chen, Jia-Rong,Xiao, Wen-Jing

supporting information; experimental part, p. 4073 - 4079 (2012/05/20)

A hydrogen-bond-mediated asymmetric [4+1] annulation/rearrangement cascade of stable sulfur ylides and nitroolefins was developed. This reaction provides a facile route to enantioenriched 4,5-substituted oxazolidinones in moderate to excellent isolated yields (65-96 %) with excellent stereocontrol (up to more than 95:5 d.r. and 97:3 e.r.). This methodology was successfully applied to the concise synthesis of two bioactive molecules. The stereocontrolled modes and mechanism have been proposed to explain the origin of this stereochemistry. Controlled cascade: A hydrogen-bond-mediated asymmetric [4+1] annulation/rearrangement cascade of stable sulfur ylides and nitroolefins was developed (see scheme). This reaction provides a facile route to enantioenriched 4,5-substituted oxazolidinones. Stereocontrolled modes and a mechanism are proposed to explain the origin of the stereochemistry. Copyright

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