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4-(2,3-epoxy-3-methylbuten-1-yl)benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1193753-08-0 Structure
  • Basic information

    1. Product Name: 4-(2,3-epoxy-3-methylbuten-1-yl)benzoic acid
    2. Synonyms: 4-(2,3-epoxy-3-methylbuten-1-yl)benzoic acid
    3. CAS NO:1193753-08-0
    4. Molecular Formula:
    5. Molecular Weight: 206.241
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1193753-08-0.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: 4-(2,3-epoxy-3-methylbuten-1-yl)benzoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(2,3-epoxy-3-methylbuten-1-yl)benzoic acid(1193753-08-0)
    11. EPA Substance Registry System: 4-(2,3-epoxy-3-methylbuten-1-yl)benzoic acid(1193753-08-0)
  • 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: 1193753-08-0(Hazardous Substances Data)

1193753-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1193753-08-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,3,7,5 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1193753-08:
(9*1)+(8*1)+(7*9)+(6*3)+(5*7)+(4*5)+(3*3)+(2*0)+(1*8)=170
170 % 10 = 0
So 1193753-08-0 is a valid CAS Registry Number.

1193753-08-0Downstream Products

1193753-08-0Relevant articles and documents

Palladium-catalyzed direct carboxylation of aryl bromides with carbon dioxide

Correa, Arkaitz,Martin, Ruben

, p. 15974 - 15975 (2009)

(Chemical Equation Presented) A novel protocol for the direct carbon dioxide insertion (CO2) into aryl halides in a catalytic manner is presented herein. Unlike other carboxylation methods using CO2, there is no need for the synthesis of the corresponding organometallic intermediates. Additionally, and in contrast to the well-established carbonylation processes, our protocol does not use highly toxic CO for the preparation of benzoic acids. Furthermore, this method is distinguished by its mild conditions, allowing the tolerance of a wide range of functional groups and substitution patterns. The crucial step of the process involves a challenging catalytic CO2 insertion into Pd-C bonds. Copyright

Process for the carboxylation of aryl halides with palladium catalysts

-

Page/Page column 9, (2011/05/04)

A process for the carboxylation of an aryl halide to yield an aryl carboxylic acid, in which the aryl halide and CO2 are contacted in an organic solvent under inert atmosphere and in the presence of a reducing agent and an adequate catalyst system.

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