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947321-82-6

4-benzyloxy-3-methoxy-2,β-dinitrostyrene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 947321-82-6 Structure

  • Basic information

    1. Product Name: 4-benzyloxy-3-methoxy-2,β-dinitrostyrene
    2. Synonyms: 4-benzyloxy-3-methoxy-2,β-dinitrostyrene
    3. CAS NO:947321-82-6
    4. Molecular Formula:
    5. Molecular Weight: 330.297
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 947321-82-6.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: 4-benzyloxy-3-methoxy-2,β-dinitrostyrene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-benzyloxy-3-methoxy-2,β-dinitrostyrene(947321-82-6)
    11. EPA Substance Registry System: 4-benzyloxy-3-methoxy-2,β-dinitrostyrene(947321-82-6)

  • 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: 947321-82-6(Hazardous Substances Data)

947321-82-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 947321-82-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,7,3,2 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 947321-82:
(8*9)+(7*4)+(6*7)+(5*3)+(4*2)+(3*1)+(2*8)+(1*2)=186
186 % 10 = 6
So 947321-82-6 is a valid CAS Registry Number.

947321-82-6Relevant articles and documents

Construction of the "left domain" of haplophytine

Nicolaou,Majumder, Utpal,Roche, Stephane Philippe,Chen, David Y.-K.

, p. 4715 - 4718 (2007)

(Chemical Equation Presented) Left of the middle: Synthesis of the "left" structural domain (2) of haplophytine (1) features a stereoselective construction of its sterically congested carbon-carbon bond (C9′-C15) and an efficient cascade sequence involvin

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