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phenyl[3-(3,7-dimethyl-2,6-octadienyl)-2,4,6-trihydroxyphenyl]methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76015-48-0 Structure
  • Basic information

    1. Product Name: phenyl[3-(3,7-dimethyl-2,6-octadienyl)-2,4,6-trihydroxyphenyl]methanone
    2. Synonyms:
    3. CAS NO:76015-48-0
    4. Molecular Formula:
    5. Molecular Weight: 366.457
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76015-48-0.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: phenyl[3-(3,7-dimethyl-2,6-octadienyl)-2,4,6-trihydroxyphenyl]methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: phenyl[3-(3,7-dimethyl-2,6-octadienyl)-2,4,6-trihydroxyphenyl]methanone(76015-48-0)
    11. EPA Substance Registry System: phenyl[3-(3,7-dimethyl-2,6-octadienyl)-2,4,6-trihydroxyphenyl]methanone(76015-48-0)
  • 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: 76015-48-0(Hazardous Substances Data)

76015-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76015-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,1 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76015-48:
(7*7)+(6*6)+(5*0)+(4*1)+(3*5)+(2*4)+(1*8)=120
120 % 10 = 0
So 76015-48-0 is a valid CAS Registry Number.

76015-48-0Downstream Products

76015-48-0Relevant articles and documents

Synthesis of fluorine-containing prenylated benzophenones

Mzozoyana, Vuyisa,van Heerden, Fanie R.

, p. 2226 - 2235 (2020)

In this study, an effective route to synthesize fluorine-containing prenylated benzophenones was developed. Friedel–Crafts acylation and electrophilic aromatic substitution reactions were the key reactions of this synthesis to achieve these fluorinated prenylated benzophenones. The use of DBU in the prenylation step achieved only the C-prenylated benzophenones, whereas K2CO3 produced the C- and O-prenylated benzophenones.

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