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2-benzoyl-7a-hydroxy-3-phenyloctahydrobenzofuran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97800-01-6

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  • 97800-01-6 Structure
  • Basic information

    1. Product Name: 2-benzoyl-7a-hydroxy-3-phenyloctahydrobenzofuran
    2. Synonyms:
    3. CAS NO:97800-01-6
    4. Molecular Formula:
    5. Molecular Weight: 322.404
    6. EINECS: N/A
    7. Product Categories: N/A
  • 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-benzoyl-7a-hydroxy-3-phenyloctahydrobenzofuran(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-benzoyl-7a-hydroxy-3-phenyloctahydrobenzofuran(97800-01-6)
    11. EPA Substance Registry System: 2-benzoyl-7a-hydroxy-3-phenyloctahydrobenzofuran(97800-01-6)
  • 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: 97800-01-6(Hazardous Substances Data)

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97800-01-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97800-01-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,8,0 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 97800-01:
(7*9)+(6*7)+(5*8)+(4*0)+(3*0)+(2*0)+(1*1)=146
146 % 10 = 6
So 97800-01-6 is a valid CAS Registry Number.

97800-01-6Downstream Products

97800-01-6Relevant academic research and scientific papers

CHEMISTRY OF 1,5-DIKETONE DERIVATIVES. 1. OXIDATION OF 8a-METHOXY-4a,5,6,7,8,8a-HEXAHYDROCHROMENES BY MONOPERPHTHALIC ACID

Moskovkina, T. V.,Vysotskii, V. I.,Tilichenko, M. N.

, p. 142 - 147 (1985)

2-(2-Oxo-3-hydroxy-1,3-diphenylpropyl)cyclohexanone, 2-(2,3-dioxo-1,3-diphenylpropyl)cyclohexanone, and 2-benzyl-7a-hydroxy-3-phenylperhydrobenzofuran are formed by the action of monoperphthalic acid on 8a-methoxy-2,4-diphenyl-4a,5,6,7,8,8a-hexahydrochromene.Under analogous conditions, 4a-methoxy-10-phenyl-1,2,3,4,4a,6,7,8,9,10a-decahydroxanthene forms 7a-hydroxy-3-phenyloctahydrobenzofuran-2-spiro-1'-cyclohexan-2'-one and its dehydration product.The behavior of the compounds obtained toward acetic anhydride and a methanolic solution of HCl was studied.The configurations of the reaction products and the reaction path are considered.

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