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211935-26-1

2-Benzyloxy-1-methoxy-3-(3-nitropropyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 211935-26-1 Structure

  • Basic information

    1. Product Name: 2-Benzyloxy-1-methoxy-3-(3-nitropropyl)benzene
    2. Synonyms: 2-Benzyloxy-1-methoxy-3-(3-nitropropyl)benzene
    3. CAS NO:211935-26-1
    4. Molecular Formula:
    5. Molecular Weight: 301.342
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 211935-26-1.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: 2-Benzyloxy-1-methoxy-3-(3-nitropropyl)benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Benzyloxy-1-methoxy-3-(3-nitropropyl)benzene(211935-26-1)
    11. EPA Substance Registry System: 2-Benzyloxy-1-methoxy-3-(3-nitropropyl)benzene(211935-26-1)

  • 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: 211935-26-1(Hazardous Substances Data)

211935-26-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 211935-26-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,9,3 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 211935-26:
(8*2)+(7*1)+(6*1)+(5*9)+(4*3)+(3*5)+(2*2)+(1*6)=111
111 % 10 = 1
So 211935-26-1 is a valid CAS Registry Number.

211935-26-1Relevant articles and documents

Synthesis of the bisbenzannelated spiroketal core of the γ-rubromycins. The use of a novel Nef-type reaction mediated by Pearlman's catalyst

Capecchi, Tanya,De Koning, Charles B.,Michael, Joseph P.

, p. 2681 - 2688 (2007/10/03)

The synthesis of the bisbenzannelated spiroketal core 6 of γ-rubromycin 1 from the substituted nitrostyrene 20 was achieved by using a novel Nef-type reaction mediated by Pearlman's catalyst. The precursor 28 was synthesised from readily prepared starting materials using Henry condensation chemistry. The product 6 was found to exist in two conformations in solution as shown by NMR spectroscopy.

Nitroalkenes as precursors to the aromatic spiroketal skeleton of γ- rubromycin. A Nef-type reaction mediated by Pearlman's catalyst

Capecchi, Tanya,De Koning, Charles B.,Michael, Joseph P.

, p. 5429 - 5432 (2007/10/03)

The first synthesis of the benzannelated spiroketal core of γ- rubromycin using Henry condensations and a novel Nef-type reaction induced by Pearlman's catalyst is described.

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