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118510-02-4

(E)-2-methoxy-1-nitro-4-(2-nitroethenyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 118510-02-4 Structure

  • Basic information

    1. Product Name: (E)-2-methoxy-1-nitro-4-(2-nitroethenyl)benzene
    2. Synonyms:
    3. CAS NO:118510-02-4
    4. Molecular Formula:
    5. Molecular Weight: 224.173
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 118510-02-4.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: (E)-2-methoxy-1-nitro-4-(2-nitroethenyl)benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-2-methoxy-1-nitro-4-(2-nitroethenyl)benzene(118510-02-4)
    11. EPA Substance Registry System: (E)-2-methoxy-1-nitro-4-(2-nitroethenyl)benzene(118510-02-4)

  • 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: 118510-02-4(Hazardous Substances Data)

118510-02-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118510-02-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,5,1 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 118510-02:
(8*1)+(7*1)+(6*8)+(5*5)+(4*1)+(3*0)+(2*0)+(1*2)=94
94 % 10 = 4
So 118510-02-4 is a valid CAS Registry Number.

118510-02-4Relevant articles and documents

Synthesis of vinylphosphonates and its first exploration of bioactivity

Li, Sheng-Nan,Xu, Lan-Ting,Chenb, Yue,Lia, Ju-Lian,He, Ling

experimental part, p. 416 - 422 (2012/05/04)

Phosphonation of β-nitro-alkene with triethyl phosphite was achieved under microwave irradiation using CH2Cl2 as the solvent in the absence of catalyst with moderate to high yields (up to 90%). This method of formation of carbonphosphor bonds is simple, mild, convenient and effective. Synchronously, a number of vinylphosphonates derivatives were synthesized and evaluated biologically preliminary.

Cerium(IV)-induced nitration of cinnamic acids. Novel remote electrophilic substitution

Peterson, John R.,Do, Hoang D.,Dunham, Andrew J.

, p. 1670 - 1674 (2007/10/02)

The treatment of (E)-3,4-dimethoxycinnamic acid with ceric amonium nitrate in trifluoroacetic acid afforded (E)1,2-dimethoxy-4-nitro-5-(2-nitroethenyl)benzene in 79percent yield.The unusual ipso substitution of the carboxylic acid moiety by a nitro functional center illustrated a new reaction manifold of cerium(IV).Six cinnamic acids were examined to ascertain the generality of the transformation.The bidentate nitrato structure of the metal salt is believed to account for the nitrating ability of this system.

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