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620167-52-4

2-Cyclohexen-1-one, 2-[[2-bromo-3-methoxy-4-(phenylmethoxy)phenyl]methyl]-3-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 620167-52-4 Structure

  • Basic information

    1. Product Name: 2-Cyclohexen-1-one, 2-[[2-bromo-3-methoxy-4-(phenylmethoxy)phenyl]methyl]-3-methyl-
    2. Synonyms:
    3. CAS NO:620167-52-4
    4. Molecular Formula: C22H23BrO3
    5. Molecular Weight: 415.327
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 620167-52-4.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: 2-Cyclohexen-1-one, 2-[[2-bromo-3-methoxy-4-(phenylmethoxy)phenyl]methyl]-3-methyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Cyclohexen-1-one, 2-[[2-bromo-3-methoxy-4-(phenylmethoxy)phenyl]methyl]-3-methyl-(620167-52-4)
    11. EPA Substance Registry System: 2-Cyclohexen-1-one, 2-[[2-bromo-3-methoxy-4-(phenylmethoxy)phenyl]methyl]-3-methyl-(620167-52-4)

  • 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: 620167-52-4(Hazardous Substances Data)

620167-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 620167-52-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,0,1,6 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 620167-52:
(8*6)+(7*2)+(6*0)+(5*1)+(4*6)+(3*7)+(2*5)+(1*2)=124
124 % 10 = 4
So 620167-52-4 is a valid CAS Registry Number.

620167-52-4Relevant articles and documents

General route to 4a-methylhydrofluorene diterpenoids: Total syntheses of (±)-taiwaniaquinones D and H, (±)-taiwaniaquinol B, (±)-dichroanal B, and (±)-dichroanone

Banerjee, Mainak,Mukhopadhyay, Ranjan,Achari, Basudeb,Banerjee, Asish Kr.

, p. 2787 - 2796 (2007/10/03)

A general and convergent route for the synthesis of the 4a-methylhydrofluorene diterpenoids has been established through a common hexahydrofluorenone intermediate (10) obtained via Pd(0)-catalyzed reductive cyclization of a substituted 2-(2-bromobenzyl) methylene cyclohexane (13). The strategy has been successfully utilized for the synthesis of (±)-taiwaniaquinones D (3) and H (5), (±)-taiwaniaquinol B (1), (±)-dichroanal B (7), and (±)-dichroanone (8).

Intramolecular Heck reaction strategy for the synthesis of functionalised tetrahydroanthracenes: A facile formal total synthesis of the linear abietane diterpene, umbrosone

Sengupta, Sujaya,Mukhopadhyay, Ranjan,Achari, Basudeb,Banerjee, Asish Kr.

, p. 1515 - 1519 (2007/10/03)

Rapid annulation employing an intramolecular Heck reaction yielded the functionalised 1,1,10-trimethyl-6-methoxy-1,2,3,4-tetrahydroanthracene 4a, a key intermediate for the linear diterpenoid quinone umbrosone (1), and the related compounds 4b-d. A simila

First Total Synthesis of the 4a-Methyltetrahydrofluorene Diterpenoids (±)-Dichroanal B and (±)-Dichroanone

Banerjee, Mainak,Mukhopadhyay, Ranjan,Achari, Basudeb,Banerjee, Asish Kr.

, p. 3931 - 3933 (2007/10/03)

(Matrix presented) A simple synthesis of the 4a-methyltetrahydrofluorene diterpenoids (±)-dichroanal B and (±)-dichroanone has been achieved through a common hexahydrofluorenone intermediate obtained via Pd(0)-catalyzed reductive cyclization of a substituted 2-(2-bromobenzyl) methylene cyclohexane.

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