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cyclohexyl methyl ketone [4-(trifluoromethyl)phenyl]hydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1146398-27-7 Structure
  • Basic information

    1. Product Name: cyclohexyl methyl ketone [4-(trifluoromethyl)phenyl]hydrazone
    2. Synonyms:
    3. CAS NO:1146398-27-7
    4. Molecular Formula:
    5. Molecular Weight: 284.324
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1146398-27-7.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: cyclohexyl methyl ketone [4-(trifluoromethyl)phenyl]hydrazone(CAS DataBase Reference)
    10. NIST Chemistry Reference: cyclohexyl methyl ketone [4-(trifluoromethyl)phenyl]hydrazone(1146398-27-7)
    11. EPA Substance Registry System: cyclohexyl methyl ketone [4-(trifluoromethyl)phenyl]hydrazone(1146398-27-7)
  • 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: 1146398-27-7(Hazardous Substances Data)

1146398-27-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1146398-27-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,6,3,9 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1146398-27:
(9*1)+(8*1)+(7*4)+(6*6)+(5*3)+(4*9)+(3*8)+(2*2)+(1*7)=167
167 % 10 = 7
So 1146398-27-7 is a valid CAS Registry Number.

1146398-27-7Downstream Products

1146398-27-7Relevant articles and documents

Photoreversible Zn2+ ion transportation across an interface using ion-chelating substituted photochromic 3,3′-indolospirobenzopyrans: Steric and electronic controlling effects

Roxburgh, Craig J.,Sammes, Peter G.,Abdullah, Ayse

, p. 4951 - 4960 (2008)

The photoreversible transportation of Zn2+ ions across an interface using photochromic substituted-spirobenzopyrans has been demonstrated. The inclusion of strategically placed sterically influencing 3′-methyl-3b and 3-spirocyclohexyl-3c groupings is investigated and compared to the unsubstituted analogue 3a. Significant control over the spiropyran ringopening? closing reaction, and hence Zn2+ ion transportation has been realised. Additionally, the spiropyran ring-opening? closing reactions of two skeletally identical spirobenzo pyrans 4 and 5, but possessing "electronically-modifying" 5-trifluoromethyl-substitutents have been studied by 1H NMR spectroscopy: this has enabled us to realise the additional biasing, on the ring-opening?closing process, excerpted on these systems through both selectively placed, inductively controlling functional-group substitution and/or, simultaneously, sterically influencing group substitution. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

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