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2-bromo-3,4-dimethoxy-1-nitro-benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 861522-00-1 Structure
  • Basic information

    1. Product Name: 2-bromo-3,4-dimethoxy-1-nitro-benzene
    2. Synonyms: 2-bromo-3,4-dimethoxy-1-nitro-benzene
    3. CAS NO:861522-00-1
    4. Molecular Formula:
    5. Molecular Weight: 262.06
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 861522-00-1.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-bromo-3,4-dimethoxy-1-nitro-benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-bromo-3,4-dimethoxy-1-nitro-benzene(861522-00-1)
    11. EPA Substance Registry System: 2-bromo-3,4-dimethoxy-1-nitro-benzene(861522-00-1)
  • 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: 861522-00-1(Hazardous Substances Data)

861522-00-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 861522-00-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,1,5,2 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 861522-00:
(8*8)+(7*6)+(6*1)+(5*5)+(4*2)+(3*2)+(2*0)+(1*0)=151
151 % 10 = 1
So 861522-00-1 is a valid CAS Registry Number.

861522-00-1Relevant articles and documents

Expedient routes to valuable bromo-5,6-dimethoxyindole building blocks

Huleatt, Paul B.,Choo, Sze Shiong,Chua, Sheena,Chai, Christina L.L.

, p. 5309 - 5311 (2008)

The synthesis of 3-, 4-, 7-bromo and 4,7-dibrominated 5,6-dihydroxyindole (DHI) and 5,6-dihydroxyindole-2-carboxylic acid (DHICA) derivatives is reported. Hemetsberger and Bartoli indole syntheses were investigated and expedient routes to the desired compounds were developed. These indoles are valuable substrates for elaboration using transition metal-mediated cross-coupling chemistry.

1-Substituted-3-amino-6,7-dialkoxy-1H-1,2,4-benzothiadiazine-1-oxides

-

, (2008/06/13)

1-Substituted-3-amino-6,7-dialkoxy-1H-1,2,4-benzothiadiazine-1-oxides, useful as hypotensive agents.

1,3-Dialkyl-6,7-methoxy-1H-1,2,4-benzothiadiazine-1-oxides

-

, (2008/06/13)

1,3-Dialkyl-6,7-methoxy-1H-1,2,4-benzothiadiazine-1-oxides, useful as hypotensive agents.

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