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CAS

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78668-13-0

dibromo-3,4 dimethyl-2,6 anisole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 78668-13-0 Structure

  • Basic information

    1. Product Name: dibromo-3,4 dimethyl-2,6 anisole
    2. Synonyms: dibromo-3,4 dimethyl-2,6 anisole
    3. CAS NO:78668-13-0
    4. Molecular Formula:
    5. Molecular Weight: 293.986
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 78668-13-0.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: dibromo-3,4 dimethyl-2,6 anisole(CAS DataBase Reference)
    10. NIST Chemistry Reference: dibromo-3,4 dimethyl-2,6 anisole(78668-13-0)
    11. EPA Substance Registry System: dibromo-3,4 dimethyl-2,6 anisole(78668-13-0)

  • 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: 78668-13-0(Hazardous Substances Data)

78668-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78668-13-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,6,6 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 78668-13:
(7*7)+(6*8)+(5*6)+(4*6)+(3*8)+(2*1)+(1*3)=180
180 % 10 = 0
So 78668-13-0 is a valid CAS Registry Number.

78668-13-0Downstream Products

78668-13-0Relevant articles and documents

METABROMATION DU DIMETHYL-2,6 PHENOL ET DE SON ETHER METHYLIQUE EN MILIEU SUPERACIDE

Jacquesy, J. C.,Jouannetaud, M. P.

, p. 747 - 751 (2007/10/02)

In SbF5-HF, reaction of bromine with 2,6-dimethylphenol gives the meta bromo compound 1b which is further halogenated to 3,4-dibromo-2,6-dimethylphenol 1c.In the same conditions ether 2a yields successively 2b and 2d.Meta bromination of compounds 1a, 2a, 2b implies electrophilic attack on the O-protonated substrate, whereas reaction of the neutral phenol 1b leads to the p-bromoderivative 1c.All products are obtained in excellent yields (>85 percent).

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