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54825-95-5

(4-Isopropyl-cyclohex-1-enylmethyl)-phosphonic acid is a complex organic compound with the molecular formula C??H??O?P. It features a cyclohexene ring with an isopropyl group at the 4-position and a phosphonic acid group attached to the methylene bridge. (4-Isopropyl-cyclohex-1-enylmethyl)-phosphonic acid is characterized by its unique structure, which combines the properties of a cyclohexene ring with the reactivity of a phosphonic acid. It is a white crystalline solid and is soluble in water. Due to its chemical structure, it has potential applications in various fields, including pharmaceuticals and agrochemicals, where it may be used as an intermediate in the synthesis of more complex molecules. The compound's stability, reactivity, and potential uses make it an interesting subject for further research and development in the chemical industry.

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  • 54825-95-5 Structure

  • Basic information

    1. Product Name: (4-Isopropyl-cyclohex-1-enylmethyl)-phosphonic acid
    2. Synonyms:
    3. CAS NO:54825-95-5
    4. Molecular Formula:
    5. Molecular Weight: 218.233
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 54825-95-5.mol
    9. Article Data: 1

  • 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-Isopropyl-cyclohex-1-enylmethyl)-phosphonic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4-Isopropyl-cyclohex-1-enylmethyl)-phosphonic acid(54825-95-5)
    11. EPA Substance Registry System: (4-Isopropyl-cyclohex-1-enylmethyl)-phosphonic acid(54825-95-5)

  • 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: 54825-95-5(Hazardous Substances Data)

54825-95-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54825-95-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,2 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54825-95:
(7*5)+(6*4)+(5*8)+(4*2)+(3*5)+(2*9)+(1*5)=145
145 % 10 = 5
So 54825-95-5 is a valid CAS Registry Number.

54825-95-5Upstream product

54825-95-5Downstream Products

54825-95-5Relevant articles and documents

Natural Product-Derived Phosphonic Acids as Corrosion Inhibitors for Iron and Steel

Kipphardt, Helmut,Maison, Wolfgang,Naundorf, Tim,Ruf, Erik,Seddig, Tom

supporting information, (2022/03/23)

Organic acids, typically derived from an oil-based value chain, are frequently used as corrosion inhibitors in industrial metal working fluids. The criteria for selection of these corrosion in-hibitors have changed in the last decades, and are today not only performance-driven, but influenced by ecological considerations, toxicity and regulatory standards. We present scalable semisynthetic approaches to organic corrosion inhibitors based on phosphonic acids from renewable resources. They have been evaluated by chip filter assay, potentiodynamic polarization measurements, electrochemical impedance measurements and gravimetry for corrosion protection of iron and steel in an aqueous environment at slightly alkaline pH. The efficacy of several phosphonic acids tested was found to be strongly dependent on structural features influencing molecular self-assembly of protective layers, and the solubility of salts formed with di-and trivalent cations from the media or formed during corrosion. A carboxyphosphonic acid (derived from castor oil) was found to have remarkable anticorrosive effects in all media tested. We attribute the anticorrosion properties of this carboxyphosphonic acid to the formation of particularly stable protective layers on the metal surface. It might thus serve as a commercially attractive substitute for current acidic corrosion inhibitors, derived from renewable resources.

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