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141622-48-2

6'-phenylspiro-4'-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 141622-48-2 Structure

  • Basic information

    1. Product Name: 6'-phenylspiro-4'-one
    2. Synonyms:
    3. CAS NO:141622-48-2
    4. Molecular Formula:
    5. Molecular Weight: 294.417
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 141622-48-2.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: 6'-phenylspiro-4'-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6'-phenylspiro-4'-one(141622-48-2)
    11. EPA Substance Registry System: 6'-phenylspiro-4'-one(141622-48-2)

  • 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: 141622-48-2(Hazardous Substances Data)

141622-48-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141622-48-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,6,2 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 141622-48:
(8*1)+(7*4)+(6*1)+(5*6)+(4*2)+(3*2)+(2*4)+(1*8)=102
102 % 10 = 2
So 141622-48-2 is a valid CAS Registry Number.

141622-48-2Downstream Products

141622-48-2Relevant articles and documents

NONCONVENTIONAL FRIEDEL-CRAFTS CHEMISTRY III. ON THE REGIOSPECIFIC SYNTHESIS OF SPIRO-4'-ONE DERIVATIVES

El-Zohry, Maher F.

, p. 311 - 320 (2007/10/02)

The rection of 1-oxa-4-thiaspirononan-2-one (4) and/or 1-oxa-4-thiaspirodecan-2-one (5) with arenes (6) under the catalytic action of aluminum chloride afforded in all cases spiro-4'-ones (7a - g and 8a - g), -acetic acid, (9a - g and 10a - g), cycloalkylthioacetic acids, (11 and 20) aryl cycloalkyl sulfides, (14 and 23) diarylsulfides (15), diaryl disulfides and dicycloalkyl disulfides (13 and 22).The mechanisms of these reactions are discussed.Key words: Spiroisothiochroman-4-ones; Friedel-Crafts reactions.

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