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dimethyl (S)-2-[1-(2,4-dimethoxyphenyl)-2-nitroethyl]-2-fluoromalonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1170727-42-0 Structure
  • Basic information

    1. Product Name: dimethyl (S)-2-[1-(2,4-dimethoxyphenyl)-2-nitroethyl]-2-fluoromalonate
    2. Synonyms: dimethyl (S)-2-[1-(2,4-dimethoxyphenyl)-2-nitroethyl]-2-fluoromalonate
    3. CAS NO:1170727-42-0
    4. Molecular Formula:
    5. Molecular Weight: 359.308
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1170727-42-0.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: dimethyl (S)-2-[1-(2,4-dimethoxyphenyl)-2-nitroethyl]-2-fluoromalonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: dimethyl (S)-2-[1-(2,4-dimethoxyphenyl)-2-nitroethyl]-2-fluoromalonate(1170727-42-0)
    11. EPA Substance Registry System: dimethyl (S)-2-[1-(2,4-dimethoxyphenyl)-2-nitroethyl]-2-fluoromalonate(1170727-42-0)
  • 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: 1170727-42-0(Hazardous Substances Data)

1170727-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1170727-42-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,0,7,2 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1170727-42:
(9*1)+(8*1)+(7*7)+(6*0)+(5*7)+(4*2)+(3*7)+(2*4)+(1*2)=140
140 % 10 = 0
So 1170727-42-0 is a valid CAS Registry Number.

1170727-42-0Downstream Products

1170727-42-0Relevant articles and documents

Organocatalytic enantioselective conjugate addition of 2-fluoromalonate to nitroolefins: Direct synthesis of chiral fluorinated γ-nitro carboxylic acid derivatives

Li, Hao,Zu, Liansuo,Xie, Hexin,Wang, Wei

experimental part, p. 1525 - 1530 (2009/12/06)

An unprecedented organocatalytic asymmetric Michael addition of fluorine-containing carbon-centered nucleophiles to nitroolefins has been described. The process features the creation of a fluorine-containing quaternary carbon center and an adjacent chiral

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