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(4-hydroxy-1-phenylisophosphinoline-3-yl)-phenylmethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 304659-06-1 Structure
  • Basic information

    1. Product Name: (4-hydroxy-1-phenylisophosphinoline-3-yl)-phenylmethanone
    2. Synonyms: (4-hydroxy-1-phenylisophosphinoline-3-yl)-phenylmethanone
    3. CAS NO:304659-06-1
    4. Molecular Formula:
    5. Molecular Weight: 342.334
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 304659-06-1.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: (4-hydroxy-1-phenylisophosphinoline-3-yl)-phenylmethanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4-hydroxy-1-phenylisophosphinoline-3-yl)-phenylmethanone(304659-06-1)
    11. EPA Substance Registry System: (4-hydroxy-1-phenylisophosphinoline-3-yl)-phenylmethanone(304659-06-1)
  • 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: 304659-06-1(Hazardous Substances Data)

304659-06-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 304659-06-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,4,6,5 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 304659-06:
(8*3)+(7*0)+(6*4)+(5*6)+(4*5)+(3*9)+(2*0)+(1*6)=131
131 % 10 = 1
So 304659-06-1 is a valid CAS Registry Number.

304659-06-1Upstream product

304659-06-1Downstream Products

304659-06-1Relevant articles and documents

Organophosphorus compounds. Part 151:1 Synthesis and reactivity of a novel isophosphinoline derivative

Ruf, Sven G,Dietz, Jochen,Regitz, Manfred

, p. 6259 - 6267 (2000)

Regiospecific 1,3-dipolar cycloadditions of the carbonyl ylide 2, generated thermally from the oxirane 1, to the phosphaalkynes 3 furnish the polycyclic phosphaalkenes 4. The reaction of 4a with sulfur or gray selenium leads to the thia- or selenaphosphirane derivatives 5. An oxidation of the phosphorus atom in 5a can be achieved by the addition of a stoichiometric amount of sulfur and affords the thioxothiaphosphirane derivative 6. Thermolysis of the phosphaalkenes 4a-c gives an unexpected result: rearrangement of the ring skeleton with cleavage of the alkyl substituent at the P/C double bond to afford the isophospholine system 7 occurs. The constitution of compound 7 was deduced from its spectral data and confirmed by reactivity studies. (C) 2000 Elsevier Science Ltd.

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