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100610-99-9

4-methoxycyclohexanone (2,4-dinitrophenyl)hydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 100610-99-9 Structure

  • Basic information

    1. Product Name: 4-methoxycyclohexanone (2,4-dinitrophenyl)hydrazone
    2. Synonyms:
    3. CAS NO:100610-99-9
    4. Molecular Formula:
    5. Molecular Weight: 308.294
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100610-99-9.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-methoxycyclohexanone (2,4-dinitrophenyl)hydrazone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-methoxycyclohexanone (2,4-dinitrophenyl)hydrazone(100610-99-9)
    11. EPA Substance Registry System: 4-methoxycyclohexanone (2,4-dinitrophenyl)hydrazone(100610-99-9)

  • 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: 100610-99-9(Hazardous Substances Data)

100610-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100610-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,6,1 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 100610-99:
(8*1)+(7*0)+(6*0)+(5*6)+(4*1)+(3*0)+(2*9)+(1*9)=69
69 % 10 = 9
So 100610-99-9 is a valid CAS Registry Number.

100610-99-9Downstream Products

100610-99-9Relevant articles and documents

Spectroscopic and X-ray crystallographic evidence for electrostatic effects in 4-substituted cyclohexanone-derived hydrazones, imines, and corresponding salts

Dibble, David J.,Ziller, Joseph W.,Woerpef

, p. 7706 - 7719 (2011/12/02)

The axial conformer of several 4-substituted cyclo-hexanone hydrazone salts was found to predominate in solution. Changes in the charge of the molecule and the polarity of the solvent led to changes in the conformational preference of each molecule that were consistent with electrostatic stabilization of the axial conformer. H NMR spectroscopic analysis was utilized to determine the structure of cyclohexanone-derived substrates by comparison to conformationally restricted trans-decalone derivatives and computational models. X-ray crystallography demonstrated that the axial configuration of a pendant benzyloxy group is the preferred conformation of an iminium ion in the solid state. The structure of a neutral hydrazone was also determined to favor the axial configuration for a pendant benzyloxy group in the solid state.

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