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CAS

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846567-82-6

Benzoic acid, 3-bromo-2-methoxy-6-methyl-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 846567-82-6 Structure

  • Basic information

    1. Product Name: Benzoic acid, 3-bromo-2-methoxy-6-methyl-, ethyl ester
    2. Synonyms:
    3. CAS NO:846567-82-6
    4. Molecular Formula: C11H13BrO3
    5. Molecular Weight: 273.126
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 846567-82-6.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: Benzoic acid, 3-bromo-2-methoxy-6-methyl-, ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid, 3-bromo-2-methoxy-6-methyl-, ethyl ester(846567-82-6)
    11. EPA Substance Registry System: Benzoic acid, 3-bromo-2-methoxy-6-methyl-, ethyl ester(846567-82-6)

  • 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: 846567-82-6(Hazardous Substances Data)

846567-82-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 846567-82-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,6,5,6 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 846567-82:
(8*8)+(7*4)+(6*6)+(5*5)+(4*6)+(3*7)+(2*8)+(1*2)=216
216 % 10 = 6
So 846567-82-6 is a valid CAS Registry Number.

846567-82-6Relevant articles and documents

SULPHONE COMPOUNDS AND METHODS OF MAKING AND USING SAME

-

, (2011/04/26)

The invention provides sulphone compounds and their use in treating medical disorders, such as obesity. Pharmaceutical compositions and methods of making various sulphone compounds are provided. The compounds are contemplated to have activity against methionyl aminopeptidase 2

A novel synthesis of bromomethoxy disubstituted derivatives of benzocyclobutenone

Barve,Schiess

, p. 1729 - 1736 (2007/10/03)

Flash vacuum pyrolysis of ortho-methyl aromatic acid chlorides has been used to prepare a variety of substituted derivatives of the benzocyclobutenone ring system starting from simple precursors. The significance of the present reaction lies in the fact that the bromine atom present in the aromatic nucleus, remains undisturbed during the high temperature treatment employed in the pyrolysis and forms, a bromomethoxyketone successfully. This is an altogether new approach.

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