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352020-04-3

2-methoxy-4-bromophenol allyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 352020-04-3 Structure

  • Basic information

    1. Product Name: 2-methoxy-4-bromophenol allyl ether
    2. Synonyms: 2-methoxy-4-bromophenol allyl ether
    3. CAS NO:352020-04-3
    4. Molecular Formula:
    5. Molecular Weight: 243.1
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 352020-04-3.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-methoxy-4-bromophenol allyl ether(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-methoxy-4-bromophenol allyl ether(352020-04-3)
    11. EPA Substance Registry System: 2-methoxy-4-bromophenol allyl ether(352020-04-3)

  • 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: 352020-04-3(Hazardous Substances Data)

352020-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 352020-04-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,0,2 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 352020-04:
(8*3)+(7*5)+(6*2)+(5*0)+(4*2)+(3*0)+(2*0)+(1*4)=83
83 % 10 = 3
So 352020-04-3 is a valid CAS Registry Number.

352020-04-3Relevant articles and documents

A short-step asymmetric synthesis of dehydrodiconiferyl alcohol via C-H insertion reaction

Matsumoto, Shogo,Asakawa, Tomohiro,Hamashima, Yoshitaka,Kan, Toshiyuki

, p. 1082 - 1084 (2012)

A rhodium-catalyzed intramolecular C-H insertion reaction using a chiral auxiliary and a chiral catalyst was employed to achieve double asymmetric induction of a trans-disubstituted dihydrobenzofuran ring, as the key reaction of a stereoselective synthesis of (-)-dehydrodiconiferyl alcohol in 13 steps from commercially available guaiacol. Georg Thieme Verlag Stuttgart · New York.

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