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2-(1-phenyl-allyl)-1H-indene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 851934-07-1 Structure
  • Basic information

    1. Product Name: 2-(1-phenyl-allyl)-1H-indene
    2. Synonyms: 2-(1-phenyl-allyl)-1H-indene
    3. CAS NO:851934-07-1
    4. Molecular Formula:
    5. Molecular Weight: 232.325
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 851934-07-1.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-(1-phenyl-allyl)-1H-indene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(1-phenyl-allyl)-1H-indene(851934-07-1)
    11. EPA Substance Registry System: 2-(1-phenyl-allyl)-1H-indene(851934-07-1)
  • 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: 851934-07-1(Hazardous Substances Data)

851934-07-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 851934-07-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,9,3 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 851934-07:
(8*8)+(7*5)+(6*1)+(5*9)+(4*3)+(3*4)+(2*0)+(1*7)=181
181 % 10 = 1
So 851934-07-1 is a valid CAS Registry Number.

851934-07-1Relevant articles and documents

Towards benign synthesis of indenes from indanones: Zinc-mediated allylation of ketones in aqueous media as a source of substituted indenyl ligand precursors

Silver, Satu,Leppaenen, Ann-Sofie,Sjoeholm, Rainer,Penninkangas, Antti,Leino, Reko

, p. 1058 - 1081 (2007/10/03)

Substituted indenes are valuable ligand precursors for transition-metal complexes. Previously, most of the methods employed for the preparation of alkyl-substituted indenes have involved the use of air-sensitive organometallic lithium or Grignard reagents

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